Triple

T7168776
Position Surface form Disambiguated ID Type / Status
Subject Prescription Drug User Fee Act of 1992 E167139 entity
Predicate shortName P43 FINISHED
Object PDUFA E167139 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: PDUFA | Statement: [Prescription Drug User Fee Act of 1992, shortName, PDUFA]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: PDUFA
Context triple: [Prescription Drug User Fee Act of 1992, shortName, PDUFA]
  • A. Food and Drug Administration Amendments Act of 2007
    The Food and Drug Administration Amendments Act of 2007 is a U.S. law that expanded the FDA’s authority over drug and device safety, clinical trials, and post-market surveillance, while enhancing transparency and user fee programs.
  • B. Food and Drug Administration Safety and Innovation Act of 2012
    The Food and Drug Administration Safety and Innovation Act of 2012 is a U.S. federal law that reauthorized and expanded FDA user fee programs while enhancing the agency’s authority over drug and medical device safety, innovation, and supply chain oversight.
  • C. Prescription Drug User Fee Act of 1992 chosen
    The Prescription Drug User Fee Act of 1992 is a U.S. law that authorizes the FDA to collect fees from pharmaceutical companies to fund and expedite the review of new drug applications.
  • D. Food and Drug Administration Modernization Act of 1997
    The Food and Drug Administration Modernization Act of 1997 is a U.S. law that overhauled FDA regulatory procedures to speed the approval of drugs and medical devices while enhancing patient access to experimental therapies and modernizing agency operations.
  • E. Leahy–Smith America Invents Act
    The Leahy–Smith America Invents Act is a 2011 U.S. patent reform law that overhauled the patent system, including shifting to a first-inventor-to-file regime and creating new post-grant review procedures.
  • 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_69c68888c10c819095e0383020225758 completed March 27, 2026, 1:39 p.m.
NER Named-entity recognition batch_69c6e85c606081909f76d76fc5b90bc8 completed March 27, 2026, 8:28 p.m.
NED1 Entity disambiguation (via context triple) batch_69c7b9094a8c81909e9d5b91ec714831 completed March 28, 2026, 11:18 a.m.
Created at: March 27, 2026, 2:48 p.m.