Triple

T10790392
Position Surface form Disambiguated ID Type / Status
Subject White Oak, Maryland E254561 entity
Predicate isNearFederalFacility P22439 FINISHED
Object U.S. Food and Drug Administration Office of the Chief Scientist E392785 NE FINISHED

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: U.S. Food and Drug Administration Office of the Chief Scientist | Statement: [White Oak, Maryland, isNearFederalFacility, U.S. Food and Drug Administration Office of the Chief Scientist]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: U.S. Food and Drug Administration Office of the Chief Scientist
Context triple: [White Oak, Maryland, isNearFederalFacility, U.S. Food and Drug Administration Office of the Chief Scientist]
  • A. Office of the Chief Scientist
    The Office of the Chief Scientist is NASA’s top scientific advisory office, responsible for providing strategic scientific guidance and ensuring the integrity and coordination of the agency’s research and exploration programs.
  • B. 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.
  • 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. 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.
  • E. Office of Pharmaceutical Quality chosen
    The Office of Pharmaceutical Quality is a U.S. Food and Drug Administration office responsible for ensuring the quality, safety, and consistency of human drugs throughout their lifecycle.
  • 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_69d6aa609f008190a294200aefcb7bd5 completed April 8, 2026, 7:20 p.m.
NER Named-entity recognition batch_69d732f5b8248190a633dc44ae620a3a completed April 9, 2026, 5:02 a.m.
NED1 Entity disambiguation (via context triple) batch_69de562873b081908bea08c56b1c1e3f completed April 14, 2026, 2:58 p.m.
Created at: April 8, 2026, 9:17 p.m.