Triple
T896107
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | ISO 14971 |
E19349
|
entity |
| Predicate | relatedTo |
P37
|
FINISHED |
| Object |
IEC 60601-1
IEC 60601-1 is an international standard that specifies general 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 60601-1 | Statement: [ISO 14971, relatedTo, IEC 60601-1]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: IEC 60601-1 Context triple: [ISO 14971, relatedTo, IEC 60601-1]
-
A.
ISO 14971
ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
-
B.
IEEE Std 610.12-2010
IEEE Std 610.12-2010 is an updated IEEE standard that provides a formal glossary of terms and definitions used in software engineering.
-
C.
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.
-
D.
ISO 13485
ISO 13485 is an international quality management standard that specifies requirements for organizations involved in the design, production, installation, and servicing of medical devices and related services.
-
E.
IEC 60488
IEC 60488 is an international standard issued by the International Electrotechnical Commission that defines digital interface and command protocols for programmable measuring instruments and related control systems.
- 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 Triple: [ISO 14971, relatedTo, IEC 60601-1]
Generated description
IEC 60601-1 is an international standard that specifies general 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 60601-1 Target entity description: IEC 60601-1 is an international standard that specifies general safety and essential performance requirements for medical electrical equipment and systems.
-
A.
ISO 14971
ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
-
B.
IEEE Std 610.12-2010
IEEE Std 610.12-2010 is an updated IEEE standard that provides a formal glossary of terms and definitions used in software engineering.
-
C.
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.
-
D.
ISO 13485
ISO 13485 is an international quality management standard that specifies requirements for organizations involved in the design, production, installation, and servicing of medical devices and related services.
-
E.
IEC 60488
IEC 60488 is an international standard issued by the International Electrotechnical Commission that defines digital interface and command protocols for programmable measuring instruments and related control systems.
- 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_69a4939d37188190848be3d426ebc9ae |
completed | March 1, 2026, 7:29 p.m. |
| NER | Named-entity recognition | batch_69a4ad23d6e88190a2fb5e1e168a7b44 |
completed | March 1, 2026, 9:18 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69a7c02772208190ac86dd885728e89c |
completed | March 4, 2026, 5:16 a.m. |
| NEDg | Description generation | batch_69a7c2f036548190bc018c0cbe02d0ca |
completed | March 4, 2026, 5:28 a.m. |
| NED2 | Entity disambiguation (via description) | batch_69a7c38925b481909133a1b098b08fa9 |
completed | March 4, 2026, 5:30 a.m. |
Created at: March 1, 2026, 7:39 p.m.