Triple
T22452697
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Directive 2001/82/EC |
E555032
|
entity |
| Predicate | requires |
P100
|
FINISHED |
| Object | Member States to establish pharmacovigilance systems for veterinary medicinal products |
—
|
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: Member States to establish pharmacovigilance systems for veterinary medicinal products | Statement: [Directive 2001/82/EC, requires, Member States to establish pharmacovigilance systems for veterinary medicinal products]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Member States to establish pharmacovigilance systems for veterinary medicinal products Context triple: [Directive 2001/82/EC, requires, Member States to establish pharmacovigilance systems for veterinary medicinal products]
-
A.
Veterinary Medicinal Products Regulation
The Veterinary Medicinal Products Regulation is a European Union law that modernizes and harmonizes the rules governing the authorization, monitoring, and use of veterinary medicines across EU member states.
-
B.
Veterinary Medicines Regulations
The Veterinary Medicines Regulations are a set of UK laws that govern the authorization, manufacture, distribution, and use of veterinary medicinal products to ensure animal health, public safety, and environmental protection.
-
C.
Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC
Regulation (EU) 2019/6 is a comprehensive EU law that modernizes and harmonizes the rules governing the authorization, manufacture, distribution, and use of veterinary medicinal products across Member States.
-
D.
Committee for Medicinal Products for Veterinary Use
The Committee for Medicinal Products for Veterinary Use is the European Medicines Agency’s scientific committee responsible for evaluating and providing opinions on veterinary medicines in the European Union.
-
E.
Veterinary Medicines Directorate
The Veterinary Medicines Directorate is a UK government agency responsible for regulating veterinary medicines and ensuring their safety, quality, and effectiveness in animals and the food chain.
- 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: Member States to establish pharmacovigilance systems for veterinary medicinal products Target entity description: Member States to establish pharmacovigilance systems for veterinary medicinal products refers to the obligation on EU countries to set up mechanisms for monitoring, evaluating, and managing the safety of veterinary medicines after they are placed on the market.
-
A.
Veterinary Medicinal Products Regulation
The Veterinary Medicinal Products Regulation is a European Union law that modernizes and harmonizes the rules governing the authorization, monitoring, and use of veterinary medicines across EU member states.
-
B.
Veterinary Medicines Regulations
The Veterinary Medicines Regulations are a set of UK laws that govern the authorization, manufacture, distribution, and use of veterinary medicinal products to ensure animal health, public safety, and environmental protection.
-
C.
Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC
chosen
Regulation (EU) 2019/6 is a comprehensive EU law that modernizes and harmonizes the rules governing the authorization, manufacture, distribution, and use of veterinary medicinal products across Member States.
-
D.
Committee for Medicinal Products for Veterinary Use
The Committee for Medicinal Products for Veterinary Use is the European Medicines Agency’s scientific committee responsible for evaluating and providing opinions on veterinary medicines in the European Union.
-
E.
Veterinary Medicines Directorate
The Veterinary Medicines Directorate is a UK government agency responsible for regulating veterinary medicines and ensuring their safety, quality, and effectiveness in animals and the food chain.
- F. None of above.
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_69e11e5113208190ab58c6b595f9d1d0 |
completed | April 16, 2026, 5:37 p.m. |
| NER | Named-entity recognition | batch_69f15b4c63e88190aeedc326599edd18 |
completed | April 29, 2026, 1:13 a.m. |
Created at: April 16, 2026, 8:48 p.m.