Triple
T37724482
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | tuberous sclerosis complex |
E939680
|
entity |
| Predicate | causedByMutationIn |
P68687
|
FINISHED |
| Object |
TSC1 gene
The TSC1 gene encodes the protein hamartin, a tumor suppressor that regulates cell growth and proliferation and whose disruption is a major cause of tuberous sclerosis complex.
|
E2241410
|
NE FINISHED |
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: TSC1 gene | Statement: [tuberous sclerosis complex, causedByMutationIn, TSC1 gene]
NEDg
Description generation
gpt-5.1
Instruction
Generate a one-sentence description of the target entity. You are given a context triple in the form (subject, predicate, object), where the object is the target entity. # Instructions Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. Avoid repeating the information from the triple, unless really essential. # Response Format Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: TSC1 gene Triple: [tuberous sclerosis complex, causedByMutationIn, TSC1 gene]
Generated description
The TSC1 gene encodes the protein hamartin, a tumor suppressor that regulates cell growth and proliferation and whose disruption is a major cause of tuberous sclerosis complex.
PD
Predicate disambiguation
gpt-5-mini-2025-08-07
Target predicate: causedByMutationIn Context triple: [tuberous sclerosis complex, causedByMutationIn, TSC1 gene]
-
A.
secondaryMutation
Indicates that an additional, subsequent genetic alteration has occurred following an initial mutation in the same biological context.
-
B.
mutationAssociatedWith
chosen
Indicates that a specific genetic mutation is linked or related to another entity, such as a disease, trait, or molecular effect.
-
C.
mutationType
Indicates the specific kind or category of genetic alteration that has occurred in an entity.
-
D.
hasMutationSystem
Indicates that one entity possesses or employs a particular mutation system or mechanism for generating or managing mutations.
-
E.
stateMutationMechanism
Indicates the process or method by which a system’s state is changed from one condition to another.
- F. None of above.
Provenance (6 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_69f76edc208c8190bc8b9683f75e1024 |
completed | May 3, 2026, 3:50 p.m. |
| NER | Named-entity recognition | batch_69fd6a1c1c4881908090053bc359b181 |
completed | May 8, 2026, 4:44 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_6a40d67df1d8819090bf038521de2c5d |
completed | June 28, 2026, 8:08 a.m. |
| NEDg | Description generation | batch_6a40da63f78081908dee41d23c8d4026 |
completed | June 28, 2026, 8:25 a.m. |
| NED2 | Entity disambiguation (via description) | batch_6a40db0ab1c481909d3db018dd2b8bde |
completed | June 28, 2026, 8:27 a.m. |
| PD | Predicate disambiguation | batch_69fd696f24d8819091033afacbdaadc5 |
completed | May 8, 2026, 4:41 a.m. |
Created at: May 3, 2026, 4:18 p.m.