Triple

T4616898
Position Surface form Disambiguated ID Type / Status
Subject ISO standards E100888 entity
Predicate includeExample P1259 FINISHED
Object ISO 14971 E19349 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: ISO 14971 | Statement: [ISO standards, includeExample, ISO 14971]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: ISO 14971
Context triple: [ISO standards, includeExample, ISO 14971]
  • A. ISO 14971 chosen
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • B. ISO 13485
    ISO 13485 is an international quality management standard that specifies requirements for organizations involved in the design, production, installation, and servicing of medical devices and related services.
  • C. ICH Q9 Quality Risk Management
    ICH Q9 Quality Risk Management is an international guideline that provides a systematic, science- and risk-based approach to identifying, evaluating, and controlling quality risks throughout the lifecycle of pharmaceutical products.
  • D. ISO 10206
    ISO 10206 is an international standard that defines the Extended Pascal programming language, specifying enhancements and extensions to the original Pascal language.
  • E. IEC 60601-1
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • 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_69bd43cf363c819087fd5ab441b4a3f4 completed March 20, 2026, 12:55 p.m.
NER Named-entity recognition batch_69bd59e098c08190b769e76937dff700 completed March 20, 2026, 2:29 p.m.
NED1 Entity disambiguation (via context triple) batch_69bdfa8da23881909ba4a70e9697f260 completed March 21, 2026, 1:55 a.m.
Created at: March 20, 2026, 1:12 p.m.