Triple

T4780754
Position Surface form Disambiguated ID Type / Status
Subject IEC 60601-1 E106157 entity
Predicate isBasisFor P7051 FINISHED
Object IEC 60601-1-10
IEC 60601-1-10 is a collateral standard within the IEC 60601 series that specifies requirements for the development of physiologic closed-loop controllers used in medical electrical equipment and systems.
 E482138 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 60601-1-10 | Statement: [IEC 60601-1, isBasisFor, IEC 60601-1-10]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: IEC 60601-1-10
Context triple: [IEC 60601-1, isBasisFor, IEC 60601-1-10]
  • A. 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.
  • B. IEC 60601-1
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • C. IEC 60601-1-8
    IEC 60601-1-8 is a collateral standard within the IEC 60601 series that specifies requirements for alarm systems in medical electrical equipment and systems to ensure safe and effective clinical use.
  • D. IEC 60601-1-9
    IEC 60601-1-9 is a collateral standard within the IEC 60601 medical electrical equipment series that specifies requirements for environmentally conscious design of medical devices.
  • E. IEC 62368
    IEC 62368 is a safety standard for audio/video, information, and communication technology equipment that uses a hazard-based approach to risk assessment and protection.
  • 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 60601-1-10
Triple: [IEC 60601-1, isBasisFor, IEC 60601-1-10]
Generated description
IEC 60601-1-10 is a collateral standard within the IEC 60601 series that specifies requirements for the development of physiologic closed-loop controllers used in medical electrical equipment and systems.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07 
Target entity: IEC 60601-1-10
Target entity description: IEC 60601-1-10 is a collateral standard within the IEC 60601 series that specifies requirements for the development of physiologic closed-loop controllers used in medical electrical equipment and systems.
  • A. 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.
  • B. IEC 60601-1
    IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
  • C. IEC 60601-1-8
    IEC 60601-1-8 is a collateral standard within the IEC 60601 series that specifies requirements for alarm systems in medical electrical equipment and systems to ensure safe and effective clinical use.
  • D. IEC 60601-1-9
    IEC 60601-1-9 is a collateral standard within the IEC 60601 medical electrical equipment series that specifies requirements for environmentally conscious design of medical devices.
  • E. IEC 62368
    IEC 62368 is a safety standard for audio/video, information, and communication technology equipment that uses a hazard-based approach to risk assessment and protection.
  • 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_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_69be81a9d8f08190ac79ca210356aab4 completed March 21, 2026, 11:31 a.m.
NEDg Description generation batch_69be831104208190a594b2534584927d completed March 21, 2026, 11:37 a.m.
NED2 Entity disambiguation (via description) batch_69be8388c04c8190b9a0205fee8d9dfc completed March 21, 2026, 11:39 a.m.
Created at: March 20, 2026, 1:21 p.m.