Triple
T18750527
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | MDR |
E458512
|
entity |
| Predicate | fullName |
P16
|
FINISHED |
| Object | Regulation (EU) 2017/745 |
—
|
NE NERFINISHED |
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: Regulation (EU) 2017/745 | Statement: [MDR, fullName, Regulation (EU) 2017/745]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2017/745 Context triple: [MDR, fullName, Regulation (EU) 2017/745]
-
A.
Regulation (EU) 2017/745
chosen
Regulation (EU) 2017/745 is the European Union’s comprehensive Medical Device Regulation that modernizes and strengthens the regulatory framework for medical devices across EU member states.
-
B.
Regulation (EU) 2019/942
Regulation (EU) 2019/942 is an EU legislative act that establishes and governs the mandate, powers, and functioning of the Agency for the Cooperation of Energy Regulators (ACER) within the internal energy market.
-
C.
Regulation (EU) 2017/746 on in vitro diagnostic medical devices
Regulation (EU) 2017/746 on in vitro diagnostic medical devices is the European Union’s comprehensive legal framework governing the safety, performance, and market access of in vitro diagnostic medical devices.
-
D.
Regulation (EU) No 536/2014
Regulation (EU) No 536/2014 is the European Union’s main legal framework governing the conduct, authorization, and oversight of clinical trials on medicinal products for human use.
-
E.
Regulation (EU) No 1025/2012
Regulation (EU) No 1025/2012 is an EU legal framework that governs European standardization activities, defining how standards are developed, adopted, and used to support EU policies and the internal market.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Provenance (2 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_69d8d394dc308190b6725073f5db324c |
completed | April 10, 2026, 10:40 a.m. |
| NER | Named-entity recognition | batch_69e579ec71cc8190bb6d3fa6cca6dc8c |
completed | April 20, 2026, 12:57 a.m. |
Created at: April 10, 2026, 11:51 a.m.