Triple
T22404505
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Directive 2001/83/EC |
E553846
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | EU pharmaceutical legislation |
C14089
|
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: EU pharmaceutical legislation Context triple: [Directive 2001/83/EC, instanceOf, EU pharmaceutical legislation]
-
A.
pharmaceutical law
Pharmaceutical law is the body of legal rules and regulations governing the research, development, approval, manufacturing, marketing, distribution, and use of drugs and medical products to ensure their safety, efficacy, and ethical oversight.
-
B.
European Union regulation
A European Union regulation is a binding legislative act that applies directly and uniformly in all EU member states without needing national implementing measures, establishing common rules and standards across the Union.
-
C.
EU legal act
chosen
An EU legal act is a binding or non-binding instrument adopted by the European Union’s institutions—such as regulations, directives, decisions, recommendations, or opinions—to create, modify, or guide the application of law within the EU legal order.
-
D.
organ of the European Medicines Agency
An organ of the European Medicines Agency is a formal decision-making or advisory body within the EMA’s governance structure, such as its Management Board, Executive Director, or scientific committees, responsible for specific regulatory, administrative, or scientific functions.
-
E.
European Pharmacopoeia certificate
A European Pharmacopoeia certificate is an official document issued by the European Directorate for the Quality of Medicines & HealthCare (EDQM) confirming that a substance or product complies with the relevant monograph(s) of the European Pharmacopoeia.
- F. None of above.
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_69e11e4da7048190b4387d422a9a0de5 |
completed | April 16, 2026, 5:37 p.m. |
Created at: April 16, 2026, 8:46 p.m.