Triple

T19558437
Position Surface form Disambiguated ID Type / Status
Subject IEC 60601 E489377 entity
Predicate hasPart P35 FINISHED
Object IEC 60601-2-xx series
The IEC 60601-2-xx series is a collection of collateral and particular standards that specify detailed safety and performance requirements for specific types of medical electrical equipment under the broader IEC 60601 framework.
E1409271 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 60601-2-xx series | Statement: [IEC 60601, hasPart, IEC 60601-2-xx series]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: IEC 60601-2-xx series
Context triple: [IEC 60601, hasPart, IEC 60601-2-xx series]
  • A. IEC 60601
    IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
  • 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 60601-1-2
    IEC 60601-1-2 is an international standard specifying electromagnetic compatibility (EMC) requirements and tests for medical electrical equipment and systems to ensure safety and performance in healthcare environments.
  • D. 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.
  • E. IEC 60601-1-11
    IEC 60601-1-11 is a collateral standard specifying additional requirements for the safety and performance of medical electrical equipment and systems used in the home healthcare environment.
  • 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 60601-2-xx series
Triple: [IEC 60601, hasPart, IEC 60601-2-xx series]
Generated description
The IEC 60601-2-xx series is a collection of collateral and particular standards that specify detailed safety and performance requirements for specific types of medical electrical equipment under the broader IEC 60601 framework.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: IEC 60601-2-xx series
Target entity description: The IEC 60601-2-xx series is a collection of collateral and particular standards that specify detailed safety and performance requirements for specific types of medical electrical equipment under the broader IEC 60601 framework.
  • A. IEC 60601
    IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
  • 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 60601-1-2
    IEC 60601-1-2 is an international standard specifying electromagnetic compatibility (EMC) requirements and tests for medical electrical equipment and systems to ensure safety and performance in healthcare environments.
  • D. 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.
  • E. IEC 60601-1-11
    IEC 60601-1-11 is a collateral standard specifying additional requirements for the safety and performance of medical electrical equipment and systems used in the home healthcare environment.
  • 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_6a0815e6d7b08190a81088e91751aab8 completed May 16, 2026, 6:59 a.m.
NEDg Description generation batch_6a0817b8581c8190a3a2c9a9809f4baa completed May 16, 2026, 7:07 a.m.
NED2 Entity disambiguation (via description) batch_6a081827a09c8190bf6f4e23926f6022 completed May 16, 2026, 7:09 a.m.
Created at: April 10, 2026, 1:42 p.m.