Triple

T19558464
Position Surface form Disambiguated ID Type / Status
Subject IEC 60601 E489377 entity
Predicate relatedTo P37 FINISHED
Object IEC 62366
IEC 62366 is an international standard that specifies a usability engineering process for medical devices to ensure safe and effective use by users.
 E1384138 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 62366 | Statement: [IEC 60601, relatedTo, IEC 62366]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: IEC 62366
Context triple: [IEC 60601, relatedTo, IEC 62366]
  • A. IEC 62304
    IEC 62304 is an international standard that defines life cycle requirements for the development and maintenance of medical device software.
  • B. ISO 14971
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • C. IEC 60601-1
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • D. IEC 60601
    IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
  • E. IEC 60601-1-6
    IEC 60601-1-6 is a collateral standard in the IEC 60601 series that specifies usability engineering requirements for medical electrical equipment and systems to help ensure safety and effectiveness in clinical use.
  • 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 62366
Triple: [IEC 60601, relatedTo, IEC 62366]
Generated description
IEC 62366 is an international standard that specifies a usability engineering process for medical devices to ensure safe and effective use by users.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07 
Target entity: IEC 62366
Target entity description: IEC 62366 is an international standard that specifies a usability engineering process for medical devices to ensure safe and effective use by users.
  • A. IEC 62304
    IEC 62304 is an international standard that defines life cycle requirements for the development and maintenance of medical device software.
  • B. ISO 14971
    ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
  • C. IEC 60601-1
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • D. IEC 60601
    IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
  • E. IEC 60601-1-6
    IEC 60601-1-6 is a collateral standard in the IEC 60601 series that specifies usability engineering requirements for medical electrical equipment and systems to help ensure safety and effectiveness in clinical use.
  • 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_69d8e8dc5d8c8190a6d7bd8864f43ca0 completed April 10, 2026, 12:11 p.m.
NER Named-entity recognition batch_69e63f723d5081909553a4363b579a6b completed April 20, 2026, 3 p.m.
NED1 Entity disambiguation (via context triple) batch_6a0757809d9c8190bf7651fc9425691e completed May 15, 2026, 5:27 p.m.
NEDg Description generation batch_6a075b89f9d08190be3b14a4073fb570 completed May 15, 2026, 5:44 p.m.
NED2 Entity disambiguation (via description) batch_6a075c02150c8190b26a3d58ee68b481 completed May 15, 2026, 5:46 p.m.
Created at: April 10, 2026, 1:42 p.m.