Triple

T18750447
Position Surface form Disambiguated ID Type / Status
Subject Council Directive 93/42/EEC E458510 entity
Predicate harmonisedWith P121162 FINISHED
Object Directive 98/79/EC on in vitro diagnostic medical devices — 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 98/79/EC on in vitro diagnostic medical devices | Statement: [Council Directive 93/42/EEC, harmonisedWith, Directive 98/79/EC on in vitro diagnostic medical devices]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Directive 98/79/EC on in vitro diagnostic medical devices
Context triple: [Council Directive 93/42/EEC, harmonisedWith, Directive 98/79/EC on in vitro diagnostic medical devices]
  • A. Directive 98/79/EC on in vitro diagnostic medical devices chosen
    Directive 98/79/EC on in vitro diagnostic medical devices was an EU legal framework that set safety, performance, and conformity requirements for in vitro diagnostic medical devices placed on the European market.
  • B. Council Directive 93/42/EEC on medical devices
    Council Directive 93/42/EEC on medical devices was a key European Union legislative framework that set essential safety and performance requirements for medical devices marketed within the EU.
  • C. Council Directive 90/385/EEC on active implantable medical devices
    Council Directive 90/385/EEC on active implantable medical devices was an EU legal framework that set essential safety and performance requirements for active implantable medical devices such as pacemakers and implantable defibrillators.
  • D. Regulation (EU) 2017/746 on in vitro diagnostic medical devices
    Regulation (EU) 2017/746 on in vitro diagnostic medical devices is the European Union’s comprehensive legal framework governing the safety, performance, and market access of in vitro diagnostic medical devices.
  • E. 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.
  • 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_69d8d394dc308190b6725073f5db324c completed April 10, 2026, 10:40 a.m.
NER Named-entity recognition batch_69e579ec71cc8190bb6d3fa6cca6dc8c completed April 20, 2026, 12:57 a.m.
Created at: April 10, 2026, 11:51 a.m.