Triple

T26020777
Position Surface form Disambiguated ID Type / Status
Subject FDA Risk Evaluation and Mitigation Strategies authority E647147 entity
Predicate instanceOf P0 FINISHED
Object drug safety authority C19042 CONCEPT FINISHED

How this triple was built (1 step)

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.

CD Concept disambiguation gpt-5-mini-2025-08-07 
Target class: drug safety authority
Context triple: [FDA Risk Evaluation and Mitigation Strategies authority, instanceOf, drug safety authority]
  • A. pharmacovigilance body chosen
    A pharmacovigilance body is an organization responsible for monitoring, assessing, and preventing adverse effects or other drug-related problems to ensure the ongoing safety and effective use of medicines.
  • B. pharmacy regulator
    A pharmacy regulator is an authority or organization responsible for overseeing, licensing, and enforcing standards for pharmacies and pharmacists to ensure the safe, ethical, and effective use of medications.
  • C. center of the U.S. Food and Drug Administration
    The center of the U.S. Food and Drug Administration is the primary organizational unit within the FDA responsible for regulating and overseeing a specific category of products, such as drugs, biologics, or medical devices, to ensure their safety and effectiveness.
  • D. U.S. Food and Drug Administration center
    A U.S. Food and Drug Administration center is a specialized organizational unit within the FDA responsible for regulating and overseeing specific categories of products, such as drugs, biologics, medical devices, or food, to ensure their safety, effectiveness, and proper labeling.
  • E. organ of the European Medicines Agency
    An organ of the European Medicines Agency is a formal decision-making or advisory body within the EMA’s governance structure, such as its Management Board, Executive Director, or scientific committees, responsible for specific regulatory, administrative, or scientific functions.
  • F. None of above.

Provenance (1 batch)

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_69e77e8aa65881909ca58918f29ab2a0 completed April 21, 2026, 1:41 p.m.
Created at: April 22, 2026, 9:03 a.m.