Triple

T23233020
Position Surface form Disambiguated ID Type / Status
Subject National Music Publishers Association E581212 entity
Predicate abbreviation P43 FINISHED
Object NMPA NE NERFINISHED

How this triple was built (3 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: NMPA | Statement: [National Music Publishers Association, abbreviation, NMPA]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: NMPA
Context triple: [National Music Publishers Association, abbreviation, NMPA]
  • A. National Agency for Food and Drug Administration and Control
    The National Agency for Food and Drug Administration and Control is Nigeria’s federal regulatory body responsible for overseeing the safety, quality, and standardization of food, drugs, cosmetics, medical devices, and related products.
  • B. Food and Drug Administration (Taiwan)
    The Food and Drug Administration (Taiwan) is the national regulatory authority responsible for ensuring the safety, quality, and proper regulation of food, drugs, medical devices, and related products in Taiwan.
  • C. Committee for Proprietary Medicinal Products
    The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
  • D. Intercantonal Office for the Control of Medicines
    The Intercantonal Office for the Control of Medicines was a Swiss regulatory body responsible for overseeing the safety and quality of medicinal products before its functions were taken over at the federal level.
  • E. Pharmaceuticals and Medical Devices Agency Japan
    The Pharmaceuticals and Medical Devices Agency (PMDA) is Japan’s regulatory authority responsible for the review, approval, and safety monitoring of pharmaceuticals and medical devices.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: NMPA
Target entity description: NMPA is a U.S.-based trade association that represents the interests of music publishers and their songwriting partners in licensing, advocacy, and copyright protection.
  • A. National Agency for Food and Drug Administration and Control
    The National Agency for Food and Drug Administration and Control is Nigeria’s federal regulatory body responsible for overseeing the safety, quality, and standardization of food, drugs, cosmetics, medical devices, and related products.
  • B. Food and Drug Administration (Taiwan)
    The Food and Drug Administration (Taiwan) is the national regulatory authority responsible for ensuring the safety, quality, and proper regulation of food, drugs, medical devices, and related products in Taiwan.
  • C. Committee for Proprietary Medicinal Products
    The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
  • D. Intercantonal Office for the Control of Medicines
    The Intercantonal Office for the Control of Medicines was a Swiss regulatory body responsible for overseeing the safety and quality of medicinal products before its functions were taken over at the federal level.
  • E. Pharmaceuticals and Medical Devices Agency Japan
    The Pharmaceuticals and Medical Devices Agency (PMDA) is Japan’s regulatory authority responsible for the review, approval, and safety monitoring of pharmaceuticals and medical devices.
  • F. None of above. chosen

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_69e246043c48819089bae72c9a9c306c completed April 17, 2026, 2:39 p.m.
NER Named-entity recognition batch_69f192e70b2c8190abede6e3cd9344f7 completed April 29, 2026, 5:11 a.m.
Created at: April 17, 2026, 4:09 p.m.