Triple
T896108
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | ISO 14971 |
E19349
|
entity |
| Predicate | relatedTo |
P37
|
FINISHED |
| Object | EU Medical Device Regulation |
E100892
|
NE FINISHED |
How this triple was built (2 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: EU Medical Device Regulation | Statement: [ISO 14971, relatedTo, EU Medical Device Regulation]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: EU Medical Device Regulation Context triple: [ISO 14971, relatedTo, EU Medical Device Regulation]
-
A.
European Union medical device regulations
chosen
European Union medical device regulations are a comprehensive set of legal and technical requirements governing the safety, performance, quality management, and market approval of medical devices within EU member states.
-
B.
Regulation (EU) 1292/2013
Regulation (EU) 1292/2013 is an EU legislative act that sets out the framework, objectives, and operational rules for the European Institute of Innovation and Technology and its activities.
-
C.
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.
-
D.
ISO 14971
ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
-
E.
European Medicines Agency
The European Medicines Agency is the European Union’s regulatory authority responsible for the scientific evaluation, supervision, and safety monitoring of medicines for human and veterinary use.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Provenance (3 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. |
Created at: March 1, 2026, 7:39 p.m.