Triple

T4780719
Position Surface form Disambiguated ID Type / Status
Subject IEC 60601-1 E106157 entity
Predicate partOfSeries P1761 FINISHED
Object IEC 60601
IEC 60601 is an international series of technical standards published by the IEC that specifies 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 | Statement: [IEC 60601-1, partOfSeries, IEC 60601]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: IEC 60601
Context triple: [IEC 60601-1, partOfSeries, IEC 60601]
  • A. IEC 60601-1
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • B. IEC 62591
    IEC 62591 is an international standard that defines the WirelessHART industrial wireless communication protocol for process automation and control applications.
  • C. IEC 61334
    IEC 61334 is an international standard that defines protocols and requirements for low-speed power line communication used in utility and smart grid applications.
  • D. 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.
  • E. ISO 14971
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • 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
Triple: [IEC 60601-1, partOfSeries, IEC 60601]
Generated description
IEC 60601 is an international series of technical standards published by the IEC that specifies 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
Target entity description: IEC 60601 is an international series of technical standards published by the IEC that specifies safety and essential performance requirements for medical electrical equipment and systems.
  • A. IEC 60601-1 chosen
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • B. IEC 62591
    IEC 62591 is an international standard that defines the WirelessHART industrial wireless communication protocol for process automation and control applications.
  • C. IEC 61334
    IEC 61334 is an international standard that defines protocols and requirements for low-speed power line communication used in utility and smart grid applications.
  • D. 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.
  • E. ISO 14971
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • F. None of above.

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_69bd43f3074c8190937e7b0a457fe9f1 completed March 20, 2026, 12:56 p.m.
NER Named-entity recognition batch_69bd65aa577c81909ec1b94e47810169 completed March 20, 2026, 3:20 p.m.
NED1 Entity disambiguation (via context triple) batch_69be4d912f5c81909537b861dd0a4591 completed March 21, 2026, 7:49 a.m.
NEDg Description generation batch_69be4f483e5c8190a568a8acc19aefe3 completed March 21, 2026, 7:56 a.m.
NED2 Entity disambiguation (via description) batch_69be4fa1037881908e926df651aec812 completed March 21, 2026, 7:58 a.m.
Created at: March 20, 2026, 1:21 p.m.