Triple

T3767647
Position Surface form Disambiguated ID Type / Status
Subject Official Medicines Control Laboratories network E82717 entity
Predicate hasPart P35 FINISHED
Object Official Medicines Control Laboratory E82717 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: Official Medicines Control Laboratory | Statement: [Official Medicines Control Laboratories network, hasPart, Official Medicines Control Laboratory]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Official Medicines Control Laboratory
Context triple: [Official Medicines Control Laboratories network, hasPart, Official Medicines Control Laboratory]
  • A. Official Medicines Control Laboratories network chosen
    The Official Medicines Control Laboratories network is a European system of public laboratories that independently test and verify the quality of medicines to support regulatory authorities and protect public health.
  • B. Committee for Proprietary Medicinal Products
    The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
  • C. 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.
  • D. Center for Drug Evaluation and Research
    The Center for Drug Evaluation and Research is the U.S. FDA division responsible for overseeing the safety, effectiveness, and quality of prescription and over-the-counter drugs.
  • E. Veterinary Medicines Directorate
    The Veterinary Medicines Directorate is a UK government agency responsible for regulating veterinary medicines and ensuring their safety, quality, and effectiveness in animals and the food chain.
  • 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_69b4e5251d2481909f692937271a8013 completed March 14, 2026, 4:33 a.m.
Created at: March 8, 2026, 3:35 p.m.