Triple

T3849409
Position Surface form Disambiguated ID Type / Status
Subject Center for Drug Evaluation and Research E85252 entity
Predicate oversees P46 FINISHED
Object Office of New Drugs
The Office of New Drugs is a division within the U.S. Food and Drug Administration responsible for evaluating and regulating the safety and effectiveness of new prescription drugs before they reach the market.
E85252 NE FINISHED

How this triple was built (4 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: Office of New Drugs | Statement: [Center for Drug Evaluation and Research, oversees, Office of New Drugs]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Office of New Drugs
Context triple: [Center for Drug Evaluation and Research, oversees, Office of New Drugs]
  • A. 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.
  • 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. 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.
  • D. Food and Drug Administration
    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.
  • E. Office of Research and Development
    The Office of Research and Development is a specialized unit focused on planning, funding, and overseeing scientific and technological research initiatives within its parent organization.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NEDg Description generation gpt-5.1
Instruction
Generate a one-sentence description of the target entity. 
You are given a context triple in the form (subject, predicate, object), where the object is the target entity. 
# Instructions
Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. 
Avoid repeating the information from the triple, unless really essential.
# Response Format
Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: Office of New Drugs
Triple: [Center for Drug Evaluation and Research, oversees, Office of New Drugs]
Generated description
The Office of New Drugs is a division within the U.S. Food and Drug Administration responsible for evaluating and regulating the safety and effectiveness of new prescription drugs before they reach the market.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Office of New Drugs
Target entity description: The Office of New Drugs is a division within the U.S. Food and Drug Administration responsible for evaluating and regulating the safety and effectiveness of new prescription drugs before they reach the market.
  • A. Center for Drug Evaluation and Research chosen
    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.
  • 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. 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.
  • D. Food and Drug Administration
    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.
  • E. Office of Research and Development
    The Office of Research and Development is a specialized unit focused on planning, funding, and overseeing scientific and technological research initiatives within its parent organization.
  • F. None of above.

Provenance (5 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_69aed936de1c81908f91bed80f70abb2 completed March 9, 2026, 2:29 p.m.
NER Named-entity recognition batch_69aeebcde86081908cf3840ae002acfa completed March 9, 2026, 3:48 p.m.
NED1 Entity disambiguation (via context triple) batch_69b504172d58819089d19f5cb7b803ec completed March 14, 2026, 6:45 a.m.
NEDg Description generation batch_69b504f32da48190a561cc72f0c4e827 completed March 14, 2026, 6:49 a.m.
NED2 Entity disambiguation (via description) batch_69b5064192a48190a0f95dee872437e0 completed March 14, 2026, 6:54 a.m.
Created at: March 9, 2026, 3:19 p.m.