Triple
T4617060
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | European Union medical device regulations |
E100892
|
entity |
| Predicate | hasAbbreviation |
P43
|
FINISHED |
| Object | EU MDR |
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 MDR | Statement: [European Union medical device regulations, hasAbbreviation, EU MDR]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: EU MDR Context triple: [European Union medical device regulations, hasAbbreviation, EU MDR]
-
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.
ISO 14971
ISO 14971 is an international standard that specifies a systematic process for risk management of medical devices throughout their life cycle.
-
C.
Regulation (EU) No 1151/2012
Regulation (EU) No 1151/2012 is a European Union law that establishes the quality schemes and protection framework for agricultural products and foodstuffs, including designations such as Protected Designation of Origin and Protected Geographical Indication.
-
D.
Regulation (EU) 2018/1725
Regulation (EU) 2018/1725 is the EU law that sets out data protection rules for EU institutions, bodies, offices and agencies, aligning them with the General Data Protection Regulation (GDPR).
-
E.
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.
- 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_69bd43cf363c819087fd5ab441b4a3f4 |
completed | March 20, 2026, 12:55 p.m. |
| NER | Named-entity recognition | batch_69bd59e098c08190b769e76937dff700 |
completed | March 20, 2026, 2:29 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69bdfa8da23881909ba4a70e9697f260 |
completed | March 21, 2026, 1:55 a.m. |
Created at: March 20, 2026, 1:12 p.m.