Triple

T22404568
Position Surface form Disambiguated ID Type / Status
Subject Regulation (EU) 2019/6 E553847 entity
Predicate repeals P6257 FINISHED
Object Directive 2001/82/EC 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: Directive 2001/82/EC | Statement: [Regulation (EU) 2019/6, repeals, Directive 2001/82/EC]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Directive 2001/82/EC
Context triple: [Regulation (EU) 2019/6, repeals, Directive 2001/82/EC]
  • A. Directive 2001/82/EC chosen
    Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
  • B. Directive 2001/83/EC
    Directive 2001/83/EC is a key European Union law that sets the framework for the authorization, manufacture, distribution, and pharmacovigilance of medicinal products for human use across EU member states.
  • C. Directive 2001/104/EC
    Directive 2001/104/EC is a European Union legislative act that updates and refines the regulatory framework for medical devices originally established by Council Directive 93/42/EEC.
  • D. Directive 2008/1/EC
    Directive 2008/1/EC is a European Union directive that consolidated and updated rules on integrated pollution prevention and control for industrial installations to reduce environmental impacts.
  • E. Directive 2000/70/EC
    Directive 2000/70/EC is a European Union legislative act that updated and strengthened the regulatory framework for medical devices, particularly those incorporating stable derivatives of human blood or human plasma, within the scope of Council Directive 93/42/EEC.
  • 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_69f158b6762c8190991fc14c5ca8e609 completed April 29, 2026, 1:02 a.m.
Created at: April 16, 2026, 8:46 p.m.