Triple

T20852747
Position Surface form Disambiguated ID Type / Status
Subject European Market Infrastructure Regulation E513403 entity
Predicate wasAmendedBy P1121 FINISHED
Object Regulation (EU) 2019/834 NE NERFINISHED

How this triple was built (3 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) 2019/834 | Statement: [European Market Infrastructure Regulation, wasAmendedBy, Regulation (EU) 2019/834]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2019/834
Context triple: [European Market Infrastructure Regulation, wasAmendedBy, Regulation (EU) 2019/834]
  • 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) 2018/1139
    Regulation (EU) 2018/1139 is a key European Union legislative act that establishes the common rules and framework for civil aviation safety and the functioning of the European Union Aviation Safety Agency.
  • C. Regulation (EU) 2021/819
    Regulation (EU) 2021/819 is a European Union legal act that sets out updated rules and provisions governing the structure, mission, and functioning of the European Institute of Innovation and Technology (EIT) and its bodies.
  • D. Regulation (EU) 2021/947
    Regulation (EU) 2021/947 is the EU legal act establishing the Neighbourhood, Development and International Cooperation Instrument – Global Europe, which governs the Union’s external action financing for 2021–2027.
  • E. 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.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2019/834
Target entity description: Regulation (EU) 2019/834 is an EU legislative act that updates and simplifies the European framework for derivatives, central counterparties, and trade repositories under the European Market Infrastructure Regulation (EMIR).
  • 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) 2018/1139
    Regulation (EU) 2018/1139 is a key European Union legislative act that establishes the common rules and framework for civil aviation safety and the functioning of the European Union Aviation Safety Agency.
  • C. Regulation (EU) 2021/819
    Regulation (EU) 2021/819 is a European Union legal act that sets out updated rules and provisions governing the structure, mission, and functioning of the European Institute of Innovation and Technology (EIT) and its bodies.
  • D. Regulation (EU) 2021/947
    Regulation (EU) 2021/947 is the EU legal act establishing the Neighbourhood, Development and International Cooperation Instrument – Global Europe, which governs the Union’s external action financing for 2021–2027.
  • E. 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.
  • F. None of above. chosen

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_69e0b4f4898081908209e58edb8f9c45 completed April 16, 2026, 10:07 a.m.
NER Named-entity recognition batch_69e6c3a4df5c8190aa0e7684ad6fc9f2 completed April 21, 2026, 12:24 a.m.
Created at: April 16, 2026, 12:44 p.m.