Triple

T22693216
Position Surface form Disambiguated ID Type / Status
Subject TDP-43 proteinopathy E561103 entity
Predicate associatedWithDisease P37 FINISHED
Object frontotemporal dementia — NE NERFINISHED

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: frontotemporal dementia | Statement: [TDP-43 proteinopathy, associatedWithDisease, frontotemporal dementia]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: frontotemporal dementia
Context triple: [TDP-43 proteinopathy, associatedWithDisease, frontotemporal dementia]
  • A. Pick’s disease chosen
    Pick’s disease is a rare, progressive form of frontotemporal dementia characterized by early personality changes, behavioral disturbances, and language impairment due to degeneration of the frontal and temporal lobes of the brain.
  • B. progressive supranuclear palsy
    Progressive supranuclear palsy is a rare neurodegenerative movement disorder characterized by early postural instability, vertical gaze palsy, and cognitive and behavioral changes due to widespread tau pathology in the brain.
  • C. Neurode
    Neurode is the former German name of the town now known as Nowa Ruda in southwestern Poland.
  • D. TDP-43 proteinopathy
    TDP-43 proteinopathy is a neurodegenerative condition characterized by abnormal aggregation and mislocalization of the TDP-43 protein, commonly implicated in disorders such as amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD).
  • E. Lewy body dementia
    Lewy body dementia is a progressive neurodegenerative disorder characterized by cognitive decline, visual hallucinations, fluctuating alertness, and Parkinsonian movement symptoms, caused by abnormal protein deposits called Lewy bodies in the brain.
  • F. None of above.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

Provenance (2 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_69f1789c6ae481908975b7d27e7624ac completed April 29, 2026, 3:18 a.m.
Created at: April 17, 2026, 3:13 p.m.