Triple

T7110739
Position Surface form Disambiguated ID Type / Status
Subject FDC Act E165700 entity
Predicate abbreviation P43 FINISHED
Object FD&C Act E31160 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: FD&C Act | Statement: [FDC Act, abbreviation, FD&C Act]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: FD&C Act
Context triple: [FDC Act, abbreviation, FD&C Act]
  • A. Federal Food, Drug, and Cosmetic Act chosen
    The Federal Food, Drug, and Cosmetic Act is a key U.S. law that authorizes the Food and Drug Administration to regulate the safety, labeling, and marketing of food, drugs, medical devices, and cosmetics.
  • B. Kefauver–Harris Drug Amendments of 1962
    The Kefauver–Harris Drug Amendments of 1962 are U.S. federal regulations that strengthened drug safety and efficacy requirements, mandating proof of effectiveness and stricter oversight of pharmaceutical marketing and manufacturing.
  • C. Pure Food and Drug Act of 1906
    The Pure Food and Drug Act of 1906 was a landmark U.S. federal law that laid the foundation for modern consumer protection by prohibiting the manufacture and sale of adulterated or misbranded foods and drugs and leading to the creation of federal regulatory oversight.
  • D. Controlled Substances Act
    The Controlled Substances Act is a U.S. federal law that regulates the manufacture, distribution, and possession of certain drugs by classifying them into schedules based on their medical use and potential for abuse.
  • E. Poison Prevention Packaging Act
    The Poison Prevention Packaging Act is a U.S. federal law that requires child-resistant packaging for certain household substances to reduce the risk of accidental poisoning in children.
  • 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_69c6888120f081908f8f01b201dc4a4c completed March 27, 2026, 1:39 p.m.
NER Named-entity recognition batch_69c6e5be09d881909988b5382ffa20ed completed March 27, 2026, 8:17 p.m.
NED1 Entity disambiguation (via context triple) batch_69c7a325a07c81909bd9a8f5d4461fb9 completed March 28, 2026, 9:45 a.m.
Created at: March 27, 2026, 2:43 p.m.