Triple

T18750456
Position Surface form Disambiguated ID Type / Status
Subject Council Directive 93/42/EEC E458510 entity
Predicate repealedBy P6257 FINISHED
Object Regulation (EU) 2017/745
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.
E1341291 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) 2017/745 | Statement: [Council Directive 93/42/EEC, repealedBy, Regulation (EU) 2017/745]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2017/745
Context triple: [Council Directive 93/42/EEC, repealedBy, Regulation (EU) 2017/745]
  • A. 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.
  • 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. Regulation (EU) No 536/2014
    Regulation (EU) No 536/2014 is the European Union’s main legal framework governing the conduct, authorization, and oversight of clinical trials on medicinal products for human use.
  • D. Regulation (EU) No 1025/2012
    Regulation (EU) No 1025/2012 is an EU legal framework that governs European standardization activities, defining how standards are developed, adopted, and used to support EU policies and the internal market.
  • E. Regulation (EU) No 1307/2013
    Regulation (EU) No 1307/2013 is a key European Union law that lays down rules for direct payments to farmers under the Common Agricultural Policy, including the structure and conditions of the Basic Payment Scheme.
  • 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) 2017/745
Triple: [Council Directive 93/42/EEC, repealedBy, Regulation (EU) 2017/745]
Generated description
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.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2017/745
Target entity description: 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.
  • A. 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.
  • 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. Regulation (EU) No 536/2014
    Regulation (EU) No 536/2014 is the European Union’s main legal framework governing the conduct, authorization, and oversight of clinical trials on medicinal products for human use.
  • D. Regulation (EU) No 1025/2012
    Regulation (EU) No 1025/2012 is an EU legal framework that governs European standardization activities, defining how standards are developed, adopted, and used to support EU policies and the internal market.
  • E. Regulation (EU) No 1307/2013
    Regulation (EU) No 1307/2013 is a key European Union law that lays down rules for direct payments to farmers under the Common Agricultural Policy, including the structure and conditions of the Basic Payment Scheme.
  • 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_69d8d394dc308190b6725073f5db324c completed April 10, 2026, 10:40 a.m.
NER Named-entity recognition batch_69e579ec71cc8190bb6d3fa6cca6dc8c completed April 20, 2026, 12:57 a.m.
NED1 Entity disambiguation (via context triple) batch_6a053d36fc908190b3193d52ce4504ce completed May 14, 2026, 3:10 a.m.
NEDg Description generation batch_6a053e216ce0819093f0e9e9b707fca8 completed May 14, 2026, 3:14 a.m.
NED2 Entity disambiguation (via description) batch_6a053ed266a481908dc9ff85e1d7cf4f completed May 14, 2026, 3:17 a.m.
Created at: April 10, 2026, 11:51 a.m.