Triple

T18750395
Position Surface form Disambiguated ID Type / Status
Subject Good Manufacturing Practices E458509 entity
Predicate isRegulatedBy P1313 FINISHED
Object United States Food and Drug Administration — 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: United States Food and Drug Administration | Statement: [Good Manufacturing Practices, isRegulatedBy, United States Food and Drug Administration]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: United States Food and Drug Administration
Context triple: [Good Manufacturing Practices, isRegulatedBy, United States Food and Drug Administration]
  • A. Food and Drug Administration chosen
    The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.
  • B. Center for Biologics Evaluation and Research
    The Center for Biologics Evaluation and Research is the U.S. regulatory body responsible for overseeing the safety, efficacy, and quality of biological products such as vaccines, blood products, and gene therapies.
  • C. Center for Drug Evaluation and Research
    The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
  • D. Office of Regulatory Affairs
    The Office of Regulatory Affairs is the U.S. FDA’s primary field organization responsible for inspecting regulated products and manufacturers, enforcing compliance, and overseeing import operations to protect public health.
  • E. United States Pharmacopeia
    The United States Pharmacopeia is an official compendium that sets quality, purity, strength, and identity standards for medicines, food ingredients, and dietary supplements used in the United States and many other countries.
  • 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_69d8d394dc308190b6725073f5db324c completed April 10, 2026, 10:40 a.m.
NER Named-entity recognition batch_69e579ec71cc8190bb6d3fa6cca6dc8c completed April 20, 2026, 12:57 a.m.
Created at: April 10, 2026, 11:51 a.m.