Triple

T17354335
Position Surface form Disambiguated ID Type / Status
Subject Office of Rare Diseases Research E421895 entity
Predicate abbreviation P43 FINISHED
Object ORDR — NE ONNED1

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: ORDR | Statement: [Office of Rare Diseases Research, abbreviation, ORDR]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: ORDR
Context triple: [Office of Rare Diseases Research, abbreviation, ORDR]
  • A. ORDR chosen
    ORDR is the Office of Rare Diseases Research, a U.S. government program that coordinates and supports research, information, and collaboration related to rare diseases.
  • B. Genetic and Rare Diseases Information Center
    The Genetic and Rare Diseases Information Center is a U.S. government resource that provides reliable, up-to-date information and support to patients, families, and healthcare professionals about genetic and rare conditions.
  • C. ORPHA:2382
    ORPHA:2382 refers to Lennox-Gastaut syndrome, a rare, severe childhood-onset epileptic encephalopathy characterized by multiple seizure types, cognitive impairment, and a distinctive EEG pattern.
  • D. Office of Rare Diseases Research
    The Office of Rare Diseases Research is a U.S. government program that coordinates and supports research, information, and collaboration efforts focused on rare diseases.
  • E. Rare Diseases Registry Program
    The Rare Diseases Registry Program is an initiative that helps develop and maintain patient registries to advance research, understanding, and treatment of rare diseases.
  • 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_69d889d520008190a26917a95bf1c2ea completed April 10, 2026, 5:25 a.m.
NER Named-entity recognition batch_69e43a2f26548190a8822b2470ec3c72 completed April 19, 2026, 2:13 a.m.
NED1 Entity disambiguation (via context triple) batch_6a01955a50dc819090c1a0ec111d9fc0 in_progress May 11, 2026, 8:37 a.m.
Created at: April 10, 2026, 5:44 a.m.