Triple

T4617056
Position Surface form Disambiguated ID Type / Status
Subject European Union medical device regulations E100892 entity
Predicate hasCoreInstrument P26810 FINISHED
Object 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.
E460822 NE FINISHED

How this triple was built (4 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: [European Union medical device regulations, hasCoreInstrument, 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: [European Union medical device regulations, hasCoreInstrument, Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
  • A. 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.
  • B. 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.
  • C. Regulation (EU) 2016/794
    Regulation (EU) 2016/794 is an EU legal act that modernised and strengthened the mandate, structure, and operational framework of Europol as the Union’s law enforcement agency.
  • D. Regulation (EU) No 1151/2012
    Regulation (EU) No 1151/2012 is a European Union law that establishes the quality schemes and protection framework for agricultural products and foodstuffs, including designations such as Protected Designation of Origin and Protected Geographical Indication.
  • E. Regulation (EU) 2019/787
    Regulation (EU) 2019/787 is a European Union law that harmonizes the rules for the production, labeling, and protection of spirit drinks, including geographical indications such as Protected Designations of Origin.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NEDg Description generation gpt-5.1
Instruction
Generate a one-sentence description of the target entity. 
You are given a context triple in the form (subject, predicate, object), where the object is the target entity. 
# Instructions
Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. 
Avoid repeating the information from the triple, unless really essential.
# Response Format
Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: Regulation (EU) 2017/746 on in vitro diagnostic medical devices
Triple: [European Union medical device regulations, hasCoreInstrument, Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Generated description
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.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2017/746 on in vitro diagnostic medical devices
Target entity description: 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.
  • A. 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.
  • B. 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.
  • C. Regulation (EU) 2016/794
    Regulation (EU) 2016/794 is an EU legal act that modernised and strengthened the mandate, structure, and operational framework of Europol as the Union’s law enforcement agency.
  • D. Regulation (EU) No 1151/2012
    Regulation (EU) No 1151/2012 is a European Union law that establishes the quality schemes and protection framework for agricultural products and foodstuffs, including designations such as Protected Designation of Origin and Protected Geographical Indication.
  • E. Regulation (EU) 2019/787
    Regulation (EU) 2019/787 is a European Union law that harmonizes the rules for the production, labeling, and protection of spirit drinks, including geographical indications such as Protected Designations of Origin.
  • F. None of above. chosen

Provenance (5 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_69bd43cf363c819087fd5ab441b4a3f4 completed March 20, 2026, 12:55 p.m.
NER Named-entity recognition batch_69bd6234e8108190b985270b9ddd1f3a completed March 20, 2026, 3:05 p.m.
NED1 Entity disambiguation (via context triple) batch_69be035a44f08190900bc6898a40e4e9 completed March 21, 2026, 2:32 a.m.
NEDg Description generation batch_69be03e3e290819080ff03c0b43296fa completed March 21, 2026, 2:35 a.m.
NED2 Entity disambiguation (via description) batch_69be04af089c8190b6b0dfae4bb71b4a completed March 21, 2026, 2:38 a.m.
Created at: March 20, 2026, 1:12 p.m.