Triple
T6004682
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Survival motor neuron protein |
E133680
|
entity |
| Predicate | associatedWithDisease |
P37
|
FINISHED |
| Object | spinal muscular atrophy type II |
E24880
|
NE FINISHED |
How this triple was built (2 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: spinal muscular atrophy type II | Statement: [Survival motor neuron protein, associatedWithDisease, spinal muscular atrophy type II]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: spinal muscular atrophy type II Context triple: [Survival motor neuron protein, associatedWithDisease, spinal muscular atrophy type II]
-
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.
SMA
SMA is a radio interferometer observatory located on Maunakea in Hawaii that operates at submillimeter wavelengths to study astronomical objects such as star-forming regions, galaxies, and black holes.
-
C.
SMA
SMA is the IATA airport code for the main airport serving Santa Maria Island in the Azores, Portugal.
-
D.
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.
-
E.
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.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
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_69c00872444c8190bfaf1739dcec765c |
completed | March 22, 2026, 3:19 p.m. |
| NER | Named-entity recognition | batch_69c04f10d18081908c351170b7f58d3d |
completed | March 22, 2026, 8:20 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69c11365741c819097a43a49dd2428c1 |
completed | March 23, 2026, 10:18 a.m. |
Created at: March 22, 2026, 4:06 p.m.