Triple

T18750515
Position Surface form Disambiguated ID Type / Status
Subject Directive 98/79/EC on in vitro diagnostic medical devices E458511 entity
Predicate repealedBy P6257 FINISHED
Object Regulation (EU) 2017/746 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: Regulation (EU) 2017/746 on in vitro diagnostic medical devices | Statement: [Directive 98/79/EC on in vitro diagnostic medical devices, repealedBy, Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Regulation (EU) 2017/746 on in vitro diagnostic medical devices
Context triple: [Directive 98/79/EC on in vitro diagnostic medical devices, repealedBy, Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
  • A. Regulation (EU) 2017/746 on in vitro diagnostic medical devices chosen
    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.
  • B. Directive 98/79/EC on in vitro diagnostic medical devices
    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.
  • C. 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.
  • D. Regulation (EU) No 806/2014
    Regulation (EU) No 806/2014 is an EU law that establishes the Single Resolution Mechanism for the orderly resolution of failing banks in the euro area, including rules for the use and governance of the Single Resolution Fund.
  • E. Regulation (EU) 2018/1727
    Regulation (EU) 2018/1727 is the EU legal act that establishes and governs the functioning, mandate, and powers of Eurojust in supporting and coordinating cross-border criminal investigations and prosecutions among 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.