Triple

T896107
Position Surface form Disambiguated ID Type / Status
Subject ISO 14971 E19349 entity
Predicate relatedTo P37 FINISHED
Object IEC 60601-1
IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
E106157 NE FINISHED

How this triple was built (4 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: IEC 60601-1 | Statement: [ISO 14971, relatedTo, IEC 60601-1]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: IEC 60601-1
Context triple: [ISO 14971, relatedTo, IEC 60601-1]
  • A. ISO 14971
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • B. IEEE Std 610.12-2010
    IEEE Std 610.12-2010 is an updated IEEE standard that provides a formal glossary of terms and definitions used in software engineering.
  • C. IEEE 11073 medical device communication standards
    IEEE 11073 medical device communication standards are a family of international standards that define interoperable data exchange and integration between medical devices and healthcare information systems.
  • D. 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.
  • E. IEC 60488
    IEC 60488 is an international standard issued by the International Electrotechnical Commission that defines digital interface and command protocols for programmable measuring instruments and related control systems.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NEDg Description generation gpt-5.1
Instruction
Generate a one-sentence description of the target entity. 
You are given a context triple in the form (subject, predicate, object), where the object is the target entity. 
# Instructions
Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. 
Avoid repeating the information from the triple, unless really essential.
# Response Format
Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: IEC 60601-1
Triple: [ISO 14971, relatedTo, IEC 60601-1]
Generated description
IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: IEC 60601-1
Target entity description: IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • A. ISO 14971
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • B. IEEE Std 610.12-2010
    IEEE Std 610.12-2010 is an updated IEEE standard that provides a formal glossary of terms and definitions used in software engineering.
  • C. IEEE 11073 medical device communication standards
    IEEE 11073 medical device communication standards are a family of international standards that define interoperable data exchange and integration between medical devices and healthcare information systems.
  • D. 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.
  • E. IEC 60488
    IEC 60488 is an international standard issued by the International Electrotechnical Commission that defines digital interface and command protocols for programmable measuring instruments and related control systems.
  • F. None of above. chosen

Provenance (5 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_69a4939d37188190848be3d426ebc9ae completed March 1, 2026, 7:29 p.m.
NER Named-entity recognition batch_69a4ad23d6e88190a2fb5e1e168a7b44 completed March 1, 2026, 9:18 p.m.
NED1 Entity disambiguation (via context triple) batch_69a7c02772208190ac86dd885728e89c completed March 4, 2026, 5:16 a.m.
NEDg Description generation batch_69a7c2f036548190bc018c0cbe02d0ca completed March 4, 2026, 5:28 a.m.
NED2 Entity disambiguation (via description) batch_69a7c38925b481909133a1b098b08fa9 completed March 4, 2026, 5:30 a.m.
Created at: March 1, 2026, 7:39 p.m.