Triple

T22405271
Position Surface form Disambiguated ID Type / Status
Subject CMDv E553863 entity
Predicate appliesLaw P125 FINISHED
Object European Union legislation on veterinary medicinal products — NE NERFINISHED

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: European Union legislation on veterinary medicinal products | Statement: [CMDv, appliesLaw, European Union legislation on veterinary medicinal products]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: European Union legislation on veterinary medicinal products
Context triple: [CMDv, appliesLaw, European Union legislation on veterinary medicinal products]
  • A. European Union pharmaceutical legislation chosen
    European Union pharmaceutical legislation is the body of EU laws and regulations that governs the authorization, supervision, safety, and quality of medicines for human and veterinary use across 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. 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.
  • D. European Union animal research directives
    European Union animal research directives are a set of EU-wide legal standards that govern the ethical treatment, housing, and use of animals in scientific research, emphasizing welfare, reduction of animal use, and strict oversight.
  • 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.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

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_69e11e4da7048190b4387d422a9a0de5 completed April 16, 2026, 5:37 p.m.
NER Named-entity recognition batch_69f158b739b88190a7f1f20fd1e9b188 completed April 29, 2026, 1:02 a.m.
Created at: April 16, 2026, 8:46 p.m.