Triple

T18750459
Position Surface form Disambiguated ID Type / Status
Subject Council Directive 93/42/EEC E458510 entity
Predicate replacedBy P101 FINISHED
Object Regulation (EU) 2017/745 on 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: Regulation (EU) 2017/745 on medical devices | Statement: [Council Directive 93/42/EEC, replacedBy, Regulation (EU) 2017/745 on medical devices]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Regulation (EU) 2017/745 on medical devices
Context triple: [Council Directive 93/42/EEC, replacedBy, Regulation (EU) 2017/745 on medical devices]
  • A. Regulation (EU) 2017/745 chosen
    Regulation (EU) 2017/745 is the European Union’s comprehensive Medical Device Regulation that modernizes and strengthens the regulatory framework for medical devices across EU member states.
  • B. 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.
  • C. European Union medical device regulations
    European Union medical device regulations are a comprehensive set of legal and technical requirements governing the safety, performance, quality management, and market approval of medical devices within EU member states.
  • D. Regulation (EU) 2019/942
    Regulation (EU) 2019/942 is an EU legislative act that establishes and governs the mandate, powers, and functioning of the Agency for the Cooperation of Energy Regulators (ACER) within the internal energy market.
  • E. 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.
  • 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.