Triple

T20775675
Position Surface form Disambiguated ID Type / Status
Subject World Anti-Doping Code E511347 entity
Predicate basedOn P98 FINISHED
Object International Standard for Laboratories 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: International Standard for Laboratories | Statement: [World Anti-Doping Code, basedOn, International Standard for Laboratories]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: International Standard for Laboratories
Context triple: [World Anti-Doping Code, basedOn, International Standard for Laboratories]
  • A. International Standard for Testing and Investigations
    The International Standard for Testing and Investigations is a key technical document under the World Anti-Doping Code that sets out detailed rules and procedures for athlete testing and anti-doping investigations worldwide.
  • B. ISO 17025
    ISO 17025 is an international standard that specifies the general requirements for the competence of testing and calibration laboratories.
  • C. ILAC Mutual Recognition Arrangement
    The ILAC Mutual Recognition Arrangement is an international agreement that facilitates global acceptance of accredited laboratory and inspection results by harmonizing accreditation practices among its signatory bodies.
  • D. ISO/IEC 17000 series
    The ISO/IEC 17000 series is a family of international standards that define general requirements and principles for conformity assessment, including testing, inspection, and certification activities.
  • E. Clinical Laboratory Improvement Amendments program
    The Clinical Laboratory Improvement Amendments program is a U.S. federal regulatory framework that sets quality standards for laboratory testing on human specimens to ensure accurate, reliable, and timely patient test results.
  • 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: International Standard for Laboratories
Target entity description: The International Standard for Laboratories is a set of technical and quality requirements that govern the accreditation and operation of anti-doping laboratories worldwide.
  • A. International Standard for Testing and Investigations
    The International Standard for Testing and Investigations is a key technical document under the World Anti-Doping Code that sets out detailed rules and procedures for athlete testing and anti-doping investigations worldwide.
  • B. ISO 17025
    ISO 17025 is an international standard that specifies the general requirements for the competence of testing and calibration laboratories.
  • C. ILAC Mutual Recognition Arrangement
    The ILAC Mutual Recognition Arrangement is an international agreement that facilitates global acceptance of accredited laboratory and inspection results by harmonizing accreditation practices among its signatory bodies.
  • D. ISO/IEC 17000 series
    The ISO/IEC 17000 series is a family of international standards that define general requirements and principles for conformity assessment, including testing, inspection, and certification activities.
  • E. Clinical Laboratory Improvement Amendments program
    The Clinical Laboratory Improvement Amendments program is a U.S. federal regulatory framework that sets quality standards for laboratory testing on human specimens to ensure accurate, reliable, and timely patient test results.
  • 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_69e0b4cac7a48190a715cb3d545df2b4 completed April 16, 2026, 10:07 a.m.
NER Named-entity recognition batch_69e6c26b06ac81909aef3b0a0ad79a33 completed April 21, 2026, 12:18 a.m.
Created at: April 16, 2026, 12:37 p.m.