Triple

T18923943
Position Surface form Disambiguated ID Type / Status
Subject ATCvet E462929 entity
Predicate distinguishesFrom P278 FINISHED
Object ATC classification for human medicines NE NERFINISHED

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: ATC classification for human medicines | Statement: [ATCvet, distinguishesFrom, ATC classification for human medicines]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: ATC classification for human medicines
Context triple: [ATCvet, distinguishesFrom, ATC classification for human medicines]
  • A. Anatomical Therapeutic Chemical Classification System chosen
    The Anatomical Therapeutic Chemical Classification System is an internationally used drug classification system that organizes medicines into groups according to the organ or system they act on and their therapeutic and chemical characteristics.
  • B. World Health Organization Model List of Essential Medicines
    The World Health Organization Model List of Essential Medicines is a periodically updated catalog of the most effective, safe, and cost-efficient medicines deemed essential for meeting the priority health needs of populations worldwide.
  • C. Conditional Marketing Authorization by European Medicines Agency
    Conditional Marketing Authorization by the European Medicines Agency is a fast-track regulatory pathway that allows earlier approval of medicines, such as COVID-19 vaccines, based on less comprehensive data than normally required, provided that the benefits outweigh the risks and additional data will be supplied post-approval.
  • D. Certificates of Suitability to the monographs of the European Pharmacopoeia
    Certificates of Suitability to the monographs of the European Pharmacopoeia are official documents issued by the European Directorate for the Quality of Medicines & HealthCare (EDQM) confirming that a substance’s quality complies with the relevant European Pharmacopoeia monograph, thereby simplifying regulatory approval for medicines across Europe.
  • E. WHO Collaborating Centre for Drug Statistics Methodology
    The WHO Collaborating Centre for Drug Statistics Methodology is a specialized World Health Organization center responsible for developing and maintaining international standards for drug classification and consumption statistics, including the ATC/DDD system.
  • F. None of above.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

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_69d8dcfdbbb881909964fa5a75bd0b48 completed April 10, 2026, 11:20 a.m.
NER Named-entity recognition batch_69e5c9b549448190850d7eed4de7872b completed April 20, 2026, 6:37 a.m.
Created at: April 10, 2026, 11:59 a.m.