Triple
T5873396
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Management Board of the European Medicines Agency |
E130570
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | organ of the European Medicines Agency |
C19043
|
CONCEPT FINISHED |
How this triple was built (1 step)
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.
CD
Concept disambiguation
gpt-5-mini-2025-08-07
Target class: organ of the European Medicines Agency Context triple: [Management Board of the European Medicines Agency, instanceOf, organ of the European Medicines Agency]
-
A.
organ of the European Research Council
An organ of the European Research Council is a formal governing or advisory body within the ERC’s institutional structure that is responsible for strategic decision-making, oversight, or implementation of its research funding activities.
-
B.
organ of the Council of Europe
An organ of the Council of Europe is an institutional body established by the Council’s Statute or subsequent agreements, endowed with specific functions and powers to contribute to the organization’s objectives in democracy, human rights, and the rule of law.
-
C.
organ of the European Central Bank
An organ of the European Central Bank is a formal decision-making or advisory body established by EU law that performs specific governance, policy, or oversight functions within the ECB’s institutional framework.
-
D.
U.S. Food and Drug Administration center
A U.S. Food and Drug Administration center is a specialized organizational unit within the FDA responsible for regulating and overseeing specific categories of products, such as drugs, biologics, medical devices, or food, to ensure their safety, effectiveness, and proper labeling.
-
E.
center of the U.S. Food and Drug Administration
The center of the U.S. Food and Drug Administration is the primary organizational unit within the FDA responsible for regulating and overseeing a specific category of products, such as drugs, biologics, or medical devices, to ensure their safety and effectiveness.
- F. None of above. chosen
Provenance (1 batch)
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_69c0085047dc8190af24e311edad3c07 |
completed | March 22, 2026, 3:18 p.m. |
Created at: March 22, 2026, 3:57 p.m.