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conversion_script.py CHANGED
@@ -1,28 +1,284 @@
1
  #!/usr/bin/env python3
2
 
3
  """
4
- Run this script as ./conversion_script.py to convert the BioCause entries from
5
- the CREST v2 aggregation file to HF-compatible parquet files.
6
- """
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
7
 
8
- # 1) Install dependencies:
9
- # pip install git+https://github.com/TheMrSheldon/causality-toolkit.git
10
- # 2) Source file (fetched automatically via pandas):
11
- # - https://raw.githubusercontent.com/phosseini/CREST/master/data/crest_v2.xlsx
 
 
 
 
 
 
 
 
 
 
 
 
12
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
13
  from pathlib import Path
14
 
15
- from ctk.data.constants import Task
16
- from ctk.data.conversion import CREST2HF, CRESTSource
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
17
 
18
- converter = CREST2HF(
19
- "https://raw.githubusercontent.com/phosseini/CREST/master/data/crest_v2.xlsx",
20
- Path.cwd(),
21
- prefix="biocause",
22
- filters={"source": CRESTSource.BioCause},
23
- )
24
 
25
- for split in ["train", "dev", "test"]:
26
- converter.convert(Task.CausalityDetection, split)
27
- converter.convert(Task.CausalCandidateExtraction, split)
28
- converter.convert(Task.CausalityIdentification, split)
 
 
1
  #!/usr/bin/env python3
2
 
3
  """
4
+ Run this script as ./conversion_script.py to convert the BioCause dataset
5
+ DIRECTLY from its original brat-format annotation files, bypassing the
6
+ CREST aggregation (crest_v2.xlsx). CREST's own copy of BioCause has (a)
7
+ train only, 0 dev/test rows (a real CREST-source gap, not fixable by
8
+ adjusting causalatee's split logic), and (b) the same
9
+ idx/context character-offset misalignment already found and fixed for
10
+ CaTeRS, dropping some spans on conversion.
11
+
12
+ Citation / original source
13
+ ---------------------------
14
+ Mihaila, C., Ohta, T., Pyysalo, S., & Ananiadou, S. (2013). "BioCause:
15
+ Annotating and analysing causality in the biomedical domain." BMC
16
+ Bioinformatics, 14, 2. https://doi.org/10.1186/1471-2105-14-2
17
+ Corpus home: https://www.nactem.ac.uk/biocause/
18
+ Direct download (verified working, no login): a zip archive at
19
+ https://www.nactem.ac.uk/biocause/download-biocause-corpus.php containing
20
+ one BioCause_corpus/ directory of paired .ann/.txt files (brat standoff),
21
+ one pair per section of a PMC Open-Access article's Discussion (also
22
+ includes TIAB/Introduction/Results sections for some articles) -- 198
23
+ file pairs across 20 unique PMC article ids, verified directly.
24
+
25
+ Format: brat standoff, built on top of a pre-existing BioNLP-ST 2011
26
+ Infectious Diseases event/entity layer in the SAME .ann files (Organism,
27
+ Protein, Positive_regulation, Regulation, Gene_expression, ... -- ignored
28
+ here, we only want the Causality layer). Causal relations are event-style:
29
+ T<n> Causality <start> <end> <connective text, e.g. "resulting in">
30
+ E<n> Causality:T<n> Cause:T<a> Effect:T<b>
31
+ E<n> Causality:T<n> Effect:T<b> Evidence:T<c> (no Cause -- common)
32
+ Cause/Effect/Evidence roles always reference a T-line directly (verified:
33
+ grepped the whole corpus for a role pointing at another E-line -- none
34
+ found), so no recursive event resolution is needed. ~18 T-line spans are
35
+ discontinuous (semicolon-joined offset pairs) -- preserved via
36
+ causalatee's multi-segment entity schema.
37
+
38
+ Only 51 of 851 Causality events have an explicit Cause role; the other
39
+ 800 have Effect+Evidence with NO separate cause span at all -- the
40
+ causing participant is not marked as its own argument in those cases.
41
+ Causality-DETECTION uses all 851 (a sentence is causal if it contains ANY
42
+ Causality event, span or no span). Causal-candidate-extraction and
43
+ causality-IDENTIFICATION need an explicit (cause, effect) span pair, so
44
+ they only use the 51 Cause+Effect events -- a real, small, and worth
45
+ documenting limitation of this corpus, not an artefact of this script.
46
+
47
+ No train/dev/test split exists upstream (checked: no filename in the
48
+ archive contains train/dev/test) -- CREST's own split was entirely
49
+ invented. This script creates its own deterministic split BY ARTICLE
50
+ (not by section) so sections of the same PMC article never end up split
51
+ across train/dev/test: 14 articles -> train, 3 -> dev, 3 -> test.
52
 
53
+ Only 7 of the 20 articles contain any of the 51 Cause+Effect relations at
54
+ all (the other 13 have Effect+Evidence-only Causality events, which count
55
+ for detection but not identification/extraction -- see below). A first
56
+ version of this split just sorted article ids and sliced [:14]/[14:17]/
57
+ [17:20] -- deterministic, but blind to where those 51 relations actually
58
+ live: alphabetically, ALL THREE of the last 3 article ids happen to be
59
+ relation-free, so causality-IDENTIFICATION's test split silently ended up
60
+ with 0 usable pairs (found the hard way: the dependency-baseline runner
61
+ crashed with "BioCause has no usable identification pairs"). Fixed by
62
+ `_assign_documents_to_splits`: a
63
+ deterministic greedy assignment that places the 20 articles (sorted by
64
+ relation count descending, ties by id) one at a time into whichever split
65
+ is currently furthest below its target relation share (train/dev/test's
66
+ 14/3/3 document-count ratio), so every split ends up with a reasonable,
67
+ non-zero share of the 51 relations (currently 28/12/11) while whole
68
+ articles still never cross a split boundary.
69
 
70
+ Granularity: each row is a WHOLE SECTION (not a sentence). An earlier
71
+ version of this script cut each section into per-sentence rows (spaCy
72
+ boundaries, one row per sentence), but ~30 of BioCause's 851 Causality
73
+ events have a cause and/or effect span that references an ADJACENT
74
+ sentence rather than the one their trigger is in (discourse-level
75
+ causality, e.g. "X requires Y... [new sentence] This substitution
76
+ decreases Z") -- verified this really happens by inspecting real output.
77
+ A per-sentence schema can't represent such an event at all: either drop it
78
+ (losing ~30 real relations for no reason other than granularity) or
79
+ re-base it onto the wrong sentence's text (a real bug hit during that
80
+ attempt: a marker landing mid-word, "h<e1>istidine"). Keeping the whole
81
+ section as one unit sidesteps the tradeoff entirely -- every event's spans
82
+ are always within the row's text, nothing is dropped or corrupted. The
83
+ per-sentence view can still be derived on demand from this whole-section
84
+ data via causalatee's reusable
85
+ ``causalatee.data.utils.split_identification_to_sentences`` /
86
+ ``split_extraction_to_sentences`` utilities -- built specifically to
87
+ generalise the guard this script used to hand-roll.
88
+ """
89
+
90
+ import io
91
+ import re
92
+ import urllib.request
93
+ import zipfile
94
  from pathlib import Path
95
 
96
+ import pandas as pd
97
+
98
+ from causalatee.data.constants import ClassLabel, Relation, Task
99
+ from causalatee.data.utils import insert_entity_markers, verify_dataset
100
+
101
+ _ZIP_URL = "https://www.nactem.ac.uk/biocause/download-biocause-corpus.php"
102
+ _CACHE_DIR = Path(__file__).parent / ".cache"
103
+
104
+
105
+ def _fetch_corpus_dir() -> Path:
106
+ """Download + extract the BioCause zip once, cached under .cache/."""
107
+ corpus_dir = _CACHE_DIR / "BioCause_corpus"
108
+ if corpus_dir.is_dir() and any(corpus_dir.iterdir()):
109
+ return corpus_dir
110
+ _CACHE_DIR.mkdir(parents=True, exist_ok=True)
111
+ with urllib.request.urlopen(_ZIP_URL) as resp:
112
+ data = resp.read()
113
+ with zipfile.ZipFile(io.BytesIO(data)) as zf:
114
+ zf.extractall(_CACHE_DIR)
115
+ return corpus_dir
116
+
117
+
118
+ def _parse_ann(ann_text: str) -> tuple[dict[str, list[tuple[int, int]]], dict[str, str], list[dict]]:
119
+ """Parse one .ann file.
120
+
121
+ Returns (t_spans: T-line id -> segments, t_types: T-line id -> type,
122
+ causality_events: list of {"trigger": tid, "cause": tid|None,
123
+ "effect": tid|None} for every Causality-typed event).
124
+ """
125
+ t_spans: dict[str, list[tuple[int, int]]] = {}
126
+ t_types: dict[str, str] = {}
127
+ for line in ann_text.splitlines():
128
+ if not line.startswith("T"):
129
+ continue
130
+ tid, mid, _ = (line.split("\t", 2) + [""])[:3]
131
+ etype, offsets_str = mid.split(" ", 1)
132
+ segments = [tuple(int(x) for x in pair.split()) for pair in offsets_str.split(";")]
133
+ t_spans[tid] = sorted(segments)
134
+ t_types[tid] = etype
135
+
136
+ causality_events = []
137
+ for line in ann_text.splitlines():
138
+ if not line.startswith("E"):
139
+ continue
140
+ _, mid = line.split("\t", 1)
141
+ roles = mid.strip().split(" ")
142
+ trigger_role, trigger_tid = roles[0].split(":")
143
+ if trigger_role != "Causality":
144
+ continue
145
+ args = dict(r.split(":") for r in roles[1:] if ":" in r)
146
+ causality_events.append({
147
+ "trigger": trigger_tid,
148
+ "cause": args.get("Cause"),
149
+ "effect": args.get("Effect"),
150
+ })
151
+ return t_spans, t_types, causality_events
152
+
153
+
154
+ def _load_sections() -> list[dict]:
155
+ """One dict per .ann/.txt pair: {"doc_id", "text", "events": [...]}."""
156
+ corpus_dir = _fetch_corpus_dir()
157
+ sections = []
158
+ for ann_path in sorted(corpus_dir.glob("*.ann")):
159
+ txt_path = ann_path.with_suffix(".txt")
160
+ text = txt_path.read_text(encoding="utf-8")
161
+ t_spans, _, events = _parse_ann(ann_path.read_text(encoding="utf-8"))
162
+ doc_id = re.match(r"(PMC\d+)-", ann_path.stem).group(1)
163
+ resolved = [
164
+ {
165
+ "cause_segments": t_spans[e["cause"]] if e["cause"] else None,
166
+ "effect_segments": t_spans[e["effect"]] if e["effect"] else None,
167
+ }
168
+ for e in events
169
+ if e["effect"] in t_spans and (e["cause"] is None or e["cause"] in t_spans)
170
+ ]
171
+ sections.append({"doc_id": doc_id, "text": text, "events": resolved})
172
+ return sections
173
+
174
+
175
+ def _load_rows() -> list[dict]:
176
+ """One row per whole section, cached across the 3 convert_for_* calls.
177
+
178
+ No sentence segmentation happens here at all -- every event's
179
+ cause/effect segments are already within the section's own text by
180
+ construction, so there is nothing to re-base and nothing to drop.
181
+ """
182
+ if hasattr(_load_rows, "_cache"):
183
+ return _load_rows._cache
184
+
185
+ rows = []
186
+ for section in _load_sections():
187
+ segments: dict[str, list[tuple[int, int]]] = {}
188
+ relations = []
189
+ for i, ev in enumerate(section["events"]):
190
+ effect_id = f"e{2 * i + 1}"
191
+ segments[effect_id] = ev["effect_segments"]
192
+ if ev["cause_segments"] is not None:
193
+ cause_id = f"e{2 * i + 2}"
194
+ segments[cause_id] = ev["cause_segments"]
195
+ relations.append({"relationship": Relation.Procausal, "first": cause_id, "second": effect_id})
196
+ rows.append({"doc_id": section["doc_id"], "text": section["text"],
197
+ "relations": relations, "segments": segments})
198
+
199
+ _load_rows._cache = rows
200
+ return rows
201
+
202
+
203
+ _SPLIT_DOC_CAPACITY = {"train": 14, "dev": 3, "test": 3}
204
+
205
+
206
+ def _assign_documents_to_splits(rows: list[dict]) -> dict[str, set[str]]:
207
+ """Deterministic greedy split assignment, balanced by relation count.
208
+
209
+ Sorts articles by their number of Cause+Effect relations (descending,
210
+ ties broken by doc id), then assigns each one to whichever split still
211
+ has capacity and is currently furthest below its target relation share
212
+ (train/dev/test's document-count ratio) -- see module docstring for why
213
+ a plain sorted-id slice isn't good enough here.
214
+ """
215
+ doc_relations: dict[str, int] = {}
216
+ for r in rows:
217
+ doc_relations[r["doc_id"]] = doc_relations.get(r["doc_id"], 0) + len(r["relations"])
218
+
219
+ assigned: dict[str, set[str]] = {split: set() for split in _SPLIT_DOC_CAPACITY}
220
+ rel_totals = {split: 0 for split in _SPLIT_DOC_CAPACITY}
221
+ order = sorted(doc_relations, key=lambda d: (-doc_relations[d], d))
222
+ for doc_id in order:
223
+ candidates = [s for s, cap in _SPLIT_DOC_CAPACITY.items() if len(assigned[s]) < cap]
224
+ best = min(candidates, key=lambda s: (rel_totals[s] / _SPLIT_DOC_CAPACITY[s], -_SPLIT_DOC_CAPACITY[s]))
225
+ assigned[best].add(doc_id)
226
+ rel_totals[best] += doc_relations[doc_id]
227
+ return assigned
228
+
229
+
230
+ def _split_by_document(rows: list[dict], split: str) -> list[dict]:
231
+ wanted = _assign_documents_to_splits(rows)[split]
232
+ return [r for r in rows if r["doc_id"] in wanted]
233
+
234
+
235
+ def convert_for_causality_detection(split: str) -> None:
236
+ rows = _split_by_document(_load_rows(), split)
237
+ df = pd.DataFrame([
238
+ {
239
+ "index": f"biocause_{split}_{i}",
240
+ "text": r["text"],
241
+ "label": ClassLabel.Causal if r["relations"] or r["segments"] else ClassLabel.Uncausal,
242
+ }
243
+ for i, r in enumerate(rows)
244
+ ]).set_index("index")
245
+ for error in verify_dataset(df, Task.CausalityDetection):
246
+ print(f"WARNING [BioCause {Task.CausalityDetection}/{split}]: {error}")
247
+ df.to_parquet(f"./causality-detection/{split}.parquet", engine="pyarrow")
248
+
249
+
250
+ def convert_for_causal_candidate_extraction(split: str) -> None:
251
+ rows = _split_by_document(_load_rows(), split)
252
+ out = []
253
+ for i, r in enumerate(rows):
254
+ # Only entities that participate in a full Cause+Effect relation have a
255
+ # usable pair; entities from Effect-only (no Cause) events are dropped
256
+ # here (extraction needs no relation to exist, but we still restrict to
257
+ # spans backing an actual relation, matching the other converters'
258
+ # "only causal_eids" convention).
259
+ involved = {eid for rel in r["relations"] for eid in (rel["first"], rel["second"])}
260
+ entity = [[x for seg in r["segments"][eid] for x in seg] for eid in involved]
261
+ out.append({"index": f"biocause_{split}_{i}", "text": r["text"], "entity": entity})
262
+ df = pd.DataFrame(out).set_index("index")
263
+ for error in verify_dataset(df, Task.CausalCandidateExtraction):
264
+ print(f"WARNING [BioCause {Task.CausalCandidateExtraction}/{split}]: {error}")
265
+ df.to_parquet(f"./causal-candidate-extraction/{split}.parquet", engine="pyarrow")
266
+
267
+
268
+ def convert_for_causality_identification(split: str) -> None:
269
+ rows = _split_by_document(_load_rows(), split)
270
+ out = []
271
+ for i, r in enumerate(rows):
272
+ marked_text = insert_entity_markers(r["text"], r["segments"]) if r["segments"] else r["text"]
273
+ out.append({"index": f"biocause_{split}_{i}", "text": marked_text, "relations": r["relations"]})
274
+ df = pd.DataFrame(out).set_index("index")
275
+ for error in verify_dataset(df, Task.CausalityIdentification):
276
+ print(f"WARNING [BioCause {Task.CausalityIdentification}/{split}]: {error}")
277
+ df.to_parquet(f"./causality-identification/{split}.parquet", engine="pyarrow")
278
 
 
 
 
 
 
 
279
 
280
+ if __name__ == "__main__":
281
+ for split in ["train", "dev", "test"]:
282
+ convert_for_causality_detection(split)
283
+ convert_for_causal_candidate_extraction(split)
284
+ convert_for_causality_identification(split)