Triple
T896109
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | ISO 14971 |
E19349
|
entity |
| Predicate | relatedTo |
P37
|
FINISHED |
| Object | EU In Vitro Diagnostic 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 In Vitro Diagnostic Regulation | Statement: [ISO 14971, relatedTo, EU In Vitro Diagnostic Regulation]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: EU In Vitro Diagnostic Regulation Context triple: [ISO 14971, relatedTo, EU In Vitro Diagnostic 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.
Regulation (EC) No 726/2004
Regulation (EC) No 726/2004 is an EU law that establishes the centralized procedure for the authorization and supervision of medicinal products and defines the role and powers of the European Medicines Agency.
-
D.
Regulation (EU, Euratom) No 1141/2014
Regulation (EU, Euratom) No 1141/2014 is an EU law that establishes the rules for the recognition, funding, and oversight of European political parties and political foundations at the European level.
-
E.
European Directorate for the Quality of Medicines & HealthCare
The European Directorate for the Quality of Medicines & HealthCare is a Council of Europe body responsible for developing quality standards and guidance to ensure the safety and efficacy of medicines and improve healthcare across member states.
- 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.