license: other
license_name: cc-by-nc-sa-3.0-annotations-pubmed-texts
license_link: https://creativecommons.org/licenses/by-nc-sa/3.0/
features:
- name: input
dtype: string
- name: output
dtype: json
- name: schema
list:
- name: label
dtype: string
- name: description
dtype: string
configs:
- config_name: default
data_files:
- split: train
path: data/mlee_train.jsonl
- split: validation
path: data/mlee_validation.jsonl
- split: test
path: data/mlee_test.jsonl
MLEE (mneb format) — nested event extraction, span-linked
The Multi-Level Event Extraction corpus (Pyysalo et al., Bioinformatics 2012) converted into
the mneb json_structures event-extraction format. MLEE annotates biomedical events across
multiple levels of biological organisation — from molecular through cellular and tissue to
organism level — over PubMed abstracts on angiogenesis.
This dataset keeps event-as-argument nesting. A third of MLEE's argument links point at
another event rather than an entity, and prior conversions (including TextEE's) drop them.
Here they are kept without leaving the flat mneb record shape: every argument is a plain
{role,text,start,end} span, and an argument that points at an event carries that event's
trigger span. See Event arguments.
Char offsets are character-based and end-exclusive (input[start:end] == text).
One record = one MLEE document.
Splits
The official MLEE partition is preserved.
| Split | Records | With events | Events |
|---|---|---|---|
| train | 131 | 131 | 3,206 |
| validation | 44 | 44 | 1,102 |
| test | 87 | 87 | 2,132 |
| Total | 262 | 262 | 6,440 |
TextEE instead discards the official boundary and makes five random re-splits, so no number reported on a TextEE split is directly comparable to this one.
Record format
{
"input": "<document text>",
"output": {"json_structures": {"<event_type>": [<event>, ...]}},
"schema": []
}
An event is {"trigger": {"text","start","end"}, "arguments": [<arg>, ...]}. There is
nothing else: no type field on the event (its type is the json_structures key), and no
object nested inside an argument.
Event arguments
Every argument has the same four keys, whether it points at an entity or at another event:
{"role": "Cause", "text": "anti-VEGF neutralizing antibody", "start": 1705, "end": 1736}
{"role": "Theme", "text": "stimulated", "start": 1611, "end": 1621}
The first is an entity mention. The second is an event link: (1611, 1621) is the trigger
span of a Positive_regulation event, which is listed at the top level of the same record.
This is how mneb expresses links generally — repeat the span, no ids (cf. mneb/bc5cdr, whose
relation head/tail repeat the entity spans).
Because a linked child must be reachable, every event appears at the top level, not only the roots. To resolve links:
def resolve(js):
"""Index every event by its trigger span, then read arguments as links where they match."""
by_span = {}
for etype, evs in js.items():
for ev in evs:
by_span.setdefault((ev["trigger"]["start"], ev["trigger"]["end"]), []).append((etype, ev))
for etype, evs in js.items():
for ev in evs:
for a in ev["arguments"]:
target = by_span.get((a["start"], a["end"])) # None => entity mention
yield etype, ev, a, target
A real example from PMID-10586954 — "The insulin-conditioned RPE cell media stimulated
capillary endothelial cell proliferation, an effect that was completely blocked by anti-VEGF
neutralizing antibody". Three top-level events; the Theme chain
blocked → stimulated → proliferation is the nesting:
"Negative_regulation": [{
"trigger": {"text": "blocked", "start": 1694, "end": 1701},
"arguments": [{"role": "Theme", "text": "stimulated", "start": 1611, "end": 1621},
{"role": "Cause", "text": "anti-VEGF neutralizing antibody",
"start": 1705, "end": 1736}]}],
"Positive_regulation": [{
"trigger": {"text": "stimulated", "start": 1611, "end": 1621},
"arguments": [{"role": "Theme", "text": "proliferation", "start": 1649, "end": 1662}]}],
"Cell_proliferation": [{
"trigger": {"text": "proliferation", "start": 1649, "end": 1662},
"arguments": [{"role": "Theme", "text": "capillary endothelial cell",
"start": 1622, "end": 1648}]}]
A conversion that simply dropped event-valued arguments would say only that something was blocked by an antibody, losing that what was blocked is the stimulation of proliferation.
How faithful the span links are
- Telling a link from an entity mention: on MLEE, 0 of the 5,767 entity-valued arguments sit on a span that is also a trigger. The test "this argument's span matches a trigger span" therefore has no false positives here.
- Telling which event a link points at: 2,417 of the 2,832 links (85.3%) match exactly one event of the right type. The other 415 (14.7%) land on a trigger span shared by several same-type events, and the span cannot disambiguate them.
- Consequently 238 of the 6,678 raw
Elines (3.6%) come out byte-identical to another entry of the same type and are collapsed, leaving 6,440 events. Those are exactly the parents that differed only in an unresolvable choice of child; keeping both copies would double-count in any set-based metric.
Everything else round-trips: the offset invariant holds on every span, and the set of emitted
(type, trigger, role/span) signatures equals the same set computed straight off the raw
standoff, for every document.
Statistics
- 29 event types, 14 role types (role strings kept verbatim, so
Theme2,Participant2..4andInstrument2are not collapsed into their base role). - 8,599 raw argument links = 5,767 entity-valued + 2,832 event-valued (32.9% of all argument links are event-to-event). After the collapse above the files hold 8,155 argument instances = 5,660 entity spans + 2,495 span links.
- 2,260 events (33.9%) take at least one event argument.
- Raw nesting depth histogram
{1: 4416, 2: 1981, 3: 269, 4: 10}— max depth 4. - Nesting is almost entirely driven by the three regulation types; the sole exception is
Planned_process, which takes an event argument 9 times. OnlyThemeandCauseare ever event-linked.
Note on event counts. Two of the 6,678 raw E lines are byte-identical duplicate
annotations (PMID-16076702 E28/E29 and PMID-19540587 E11/E25 — same type, same trigger,
same arguments); they collapse under the same rule as everything else.
Full type/role inventory and nesting patterns: mlee_label_summary.md.
Browsable rendering: mlee_vis.html (open directly; data embedded, no server needed).
How this was derived
Built from the MLEE-1.0.2-rev1 standoff release (standoff/full/*.{txt,ann}), with the
official split membership taken from the filenames in
standoff/{development/train, development/test, test/test}:
- Each document's
.ann(a1 + a2 merged: entity mentions, event triggers andEevent lines) is parsed into a single text-bound annotation map. - Each
Eline becomes an event grouped under its own type;Role:T…arguments become the entity's span andRole:E…arguments become the child event's trigger span. Both come out in the same{role,text,start,end}shape. - Every event is listed at the top level, so a linked child is always resolvable. Entries that are byte-identical under one event type are then collapsed.
- Relation (
R), equivalence (*) and attribute (A/M: Negation, Speculation) lines are not carried over. Event-type and role strings are kept verbatim.
Verification built into the converter: every emitted span is re-checked against the source
text (input[start:end] == text, 0 failures); the set of emitted (type, trigger, role/span)
signatures is compared against the same set computed straight off the raw standoff and is equal
for every document; and a link audit reports, for every event-valued argument, whether its
child is uniquely identifiable from the span (the numbers quoted above).
Licence and terms of use
- Annotations are licensed under Creative Commons BY-NC-SA 3.0. This is a non-commercial, share-alike licence: derivative works must carry the same terms, and commercial use is not permitted. Please attribute by citing the paper below and linking to http://www.nactem.ac.uk/MLEE/.
- Abstracts are from PubMed, a database of the U.S. National Library of Medicine; see the NLM copyright information.
Citation
@article{Pyysalo12mlee,
author = {Sampo Pyysalo and Tomoko Ohta and Makoto Miwa and Han-Cheol Cho and
Jun'ichi Tsujii and Sophia Ananiadou},
title = {Event extraction across multiple levels of biological organization},
journal = {Bioinformatics},
volume = {28},
number = {18},
pages = {i575--i581},
year = {2012}
}