Triple
T4942686
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | IEC 60000 series |
E110974
|
entity |
| Predicate | hasPart |
P35
|
FINISHED |
| Object |
IEC 60601
IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
|
E489377
|
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 60000 series, hasPart, IEC 60601]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: IEC 60601 Context triple: [IEC 60000 series, hasPart, 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 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.
-
C.
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.
-
D.
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.
-
E.
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.
- 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 60000 series, hasPart, IEC 60601]
Generated description
IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: IEC 60601 Target entity description: IEC 60601 is an international standard that specifies safety and essential performance requirements for medical electrical equipment.
-
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 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.
-
C.
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.
-
D.
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.
-
E.
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.
- 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_69bd4415eee08190bdce70276e56a5b4 |
completed | March 20, 2026, 12:56 p.m. |
| NER | Named-entity recognition | batch_69bd70a5f56481908365d0fe16892bf4 |
completed | March 20, 2026, 4:07 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69be9c4857cc819085fbdd996134a5e8 |
completed | March 21, 2026, 1:25 p.m. |
| NEDg | Description generation | batch_69bea0b239848190a423865a4bf623f7 |
completed | March 21, 2026, 1:44 p.m. |
| NED2 | Entity disambiguation (via description) | batch_69bea13d70008190b92fa53318d30820 |
completed | March 21, 2026, 1:46 p.m. |
Created at: March 20, 2026, 1:31 p.m.