Triple
T22692921
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | FIREFISH |
E561096
|
entity |
| Predicate | investigatesIndication |
P113308
|
FINISHED |
| Object | Type 1 spinal muscular atrophy |
—
|
NE NERFINISHED |
How this triple was built (3 steps)
Every LLM step that produced this triple, in pipeline order — named-entity classification, the disambiguation choices (the exact options shown, with the pick highlighted), and the generated description. The batch + timestamp of each is in the Provenance table below.
NER
Named-entity recognition
gpt-5-mini
Instruction
Given a phrase, classify it is english named entity (e.g., persons, organizations, works of art) in Latin script, or not (e.g., literals, dates, URLs, verbose phrases). For disambiguation, the statement where the phrase occurs as object is also given. Please return a JSON object with `phrase` (string, the phrase being analyzed) and `is_ne` (boolean, indicating whether the phrase is a Named Entity).
Input
Phrase: Type 1 spinal muscular atrophy | Statement: [FIREFISH, investigatesIndication, Type 1 spinal muscular atrophy]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Type 1 spinal muscular atrophy Context triple: [FIREFISH, investigatesIndication, Type 1 spinal muscular atrophy]
-
A.
spinal muscular atrophy
chosen
Spinal muscular atrophy is a genetic neuromuscular disorder characterized by progressive muscle weakness and atrophy due to degeneration of motor neurons in the spinal cord.
-
B.
SMN1 gene
The SMN1 gene is a human gene whose proper function is critical for motor neuron survival, and mutations in it are the primary cause of spinal muscular atrophy.
-
C.
SMN2
SMN2 is a human gene that produces a backup form of survival motor neuron protein and is a key therapeutic target in spinal muscular atrophy.
-
D.
SMN complex
The SMN complex is a multiprotein assembly crucial for the biogenesis of small nuclear ribonucleoproteins (snRNPs) and proper pre-mRNA splicing, with key roles in motor neuron survival.
-
E.
5q13 (SMN1)
5q13 (SMN1) is a gene located on chromosome 5 whose proper function is critical for motor neuron survival and whose mutations are the primary cause of spinal muscular atrophy.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
PD
Predicate disambiguation
gpt-5-mini-2025-08-07
Target predicate: investigatesIndication Context triple: [FIREFISH, investigatesIndication, Type 1 spinal muscular atrophy]
-
A.
containsInvestigationOf
Indicates that one entity includes or encompasses an investigation or inquiry concerning another entity.
-
B.
areInvestigatedFor
Indicates that one or more entities are the subject of an investigation concerning a particular issue, incident, or alleged wrongdoing.
-
C.
resultOfInvestigation
Indicates that something (such as a finding, conclusion, or outcome) is produced or determined as the consequence of an investigation.
-
D.
asksToInvestigate
Indicates that one entity requests another entity to carry out an investigation into something.
-
E.
treatmentIndication
chosen
Indicates that a treatment is intended to address, alleviate, or prevent a particular condition, symptom, or medical indication.
- F. None of above.
Provenance (3 batches)
The batch behind each pipeline step, in order, with when it ran. Timestamps are batch-level — stages were processed in waves, so the object chain (NER → NED1 → NEDg → NED2) reads in order, but predicate / elicitation batches can sit in a different wave.
| Step | Stage | Batch ID | Status | When |
|---|---|---|---|---|
| creating | Elicitation | batch_69e2454d71b48190a1f80af9f82b6fcf |
completed | April 17, 2026, 2:35 p.m. |
| NER | Named-entity recognition | batch_69f1789ba0148190891781d05ec64f3c |
completed | April 29, 2026, 3:18 a.m. |
| PD | Predicate disambiguation | batch_69ee62b2259c819091ed1387a748b9f3 |
completed | April 26, 2026, 7:08 p.m. |
Created at: April 17, 2026, 3:13 p.m.