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.