Triple
T18842130
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Regulation (EU) 2017/746 on in vitro diagnostic medical devices |
E460822
|
entity |
| Predicate | establishes |
P986
|
FINISHED |
| Object | Eudamed database for in vitro diagnostic medical devices |
—
|
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: Eudamed database for in vitro diagnostic medical devices | Statement: [Regulation (EU) 2017/746 on in vitro diagnostic medical devices, establishes, Eudamed database for in vitro diagnostic medical devices]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Eudamed database for in vitro diagnostic medical devices Context triple: [Regulation (EU) 2017/746 on in vitro diagnostic medical devices, establishes, Eudamed database for in vitro diagnostic medical devices]
-
A.
European database on medical devices (EUDAMED)
chosen
The European database on medical devices (EUDAMED) is the EU’s central IT system for collecting and sharing information on medical devices and related economic operators, clinical investigations, and vigilance to support market surveillance and transparency.
-
B.
ICH E2A Clinical Safety Data Management
ICH E2A Clinical Safety Data Management is an international guideline that standardizes the collection, reporting, and evaluation of clinical safety data in drug development to support consistent pharmacovigilance and regulatory decision-making.
-
C.
BioSample database
The BioSample database is an NCBI repository that stores and organizes metadata about biological samples used in genomic and other molecular research studies.
-
D.
Dataverse
Dataverse is Microsoft's cloud-based data platform that securely stores, manages, and structures business data for use across Power Platform applications and services.
-
E.
Regenstrief Medical Record System
The Regenstrief Medical Record System is an early, pioneering electronic medical record platform that helped shape modern health informatics and clinical data management practices.
- 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_69d8dcfa11e4819090ab1ef5bdcd2b2e |
completed | April 10, 2026, 11:20 a.m. |
| NER | Named-entity recognition | batch_69e5b8eb32548190b2313e877f6ff179 |
completed | April 20, 2026, 5:26 a.m. |
Created at: April 10, 2026, 11:56 a.m.