Triple

T3767697
Position Surface form Disambiguated ID Type / Status
Subject Certificates of Suitability E82718 entity
Predicate issuedBy P29 FINISHED
Object European Directorate for the Quality of Medicines & HealthCare E12899 NE FINISHED

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: European Directorate for the Quality of Medicines & HealthCare | Statement: [Certificates of Suitability, issuedBy, European Directorate for the Quality of Medicines & HealthCare]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: European Directorate for the Quality of Medicines & HealthCare
Context triple: [Certificates of Suitability, issuedBy, European Directorate for the Quality of Medicines & HealthCare]
  • A. European Directorate for the Quality of Medicines & HealthCare chosen
    The European Directorate for the Quality of Medicines & HealthCare is a Council of Europe body responsible for developing quality standards and guidance to ensure the safety and efficacy of medicines and improve healthcare across member states.
  • B. European Medicines Agency
    The European Medicines Agency is the European Union’s regulatory authority responsible for the scientific evaluation, supervision, and safety monitoring of medicines for human and veterinary use.
  • C. Committee for Medicinal Products for Human Use
    The Committee for Medicinal Products for Human Use is the European Medicines Agency’s expert body responsible for evaluating and providing scientific opinions on the safety, quality, and efficacy of medicines for human use in the European Union.
  • D. UK Medicines and Healthcare products Regulatory Agency
    The UK Medicines and Healthcare products Regulatory Agency is the United Kingdom’s national authority responsible for regulating medicines, medical devices, and healthcare products to ensure their safety, quality, and effectiveness.
  • E. Committee for Herbal Medicinal Products
    The Committee for Herbal Medicinal Products is a scientific body within the European Medicines Agency that evaluates and provides guidance on the safety and efficacy of herbal medicines in the European Union.
  • F. None of above.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

Provenance (3 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_69ad8b207b0081909d2b48843fbd8795 completed March 8, 2026, 2:43 p.m.
NER Named-entity recognition batch_69adcc2bdf6c819088d3c6ace83ca5ea completed March 8, 2026, 7:21 p.m.
NED1 Entity disambiguation (via context triple) batch_69b4f0373bd88190aaaf45f253c4ee17 completed March 14, 2026, 5:20 a.m.
Created at: March 8, 2026, 3:35 p.m.