Triple
T5873277
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | PDCO |
E130567
|
entity |
| Predicate | legalBasis |
P125
|
FINISHED |
| Object | Regulation (EC) No 1901/2006 on medicinal products for paediatric use |
E130568
|
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: Regulation (EC) No 1901/2006 on medicinal products for paediatric use | Statement: [PDCO, legalBasis, Regulation (EC) No 1901/2006 on medicinal products for paediatric use]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Regulation (EC) No 1901/2006 on medicinal products for paediatric use Context triple: [PDCO, legalBasis, Regulation (EC) No 1901/2006 on medicinal products for paediatric use]
-
A.
Regulation (EC) No 141/2000 on orphan medicinal products
Regulation (EC) No 141/2000 on orphan medicinal products is a key European Union law that establishes incentives and a special approval framework to encourage the development and marketing of medicines for rare diseases.
-
B.
Regulation (EC) No 726/2004
Regulation (EC) No 726/2004 is an EU law that establishes the centralized procedure for the authorization and supervision of medicinal products and defines the role and powers of the European Medicines Agency.
-
C.
European Union pharmaceutical legislation
European Union pharmaceutical legislation is the body of EU laws and regulations that governs the authorization, supervision, safety, and quality of medicines for human and veterinary use across member states.
-
D.
Regulation (EU) No 1092/2010
Regulation (EU) No 1092/2010 is the EU law that established the framework for macro-prudential oversight of the financial system and created the European Systemic Risk Board to monitor and mitigate systemic risks.
-
E.
Paediatric Regulation
chosen
The Paediatric Regulation is a European Union law designed to improve the development and availability of medicines specifically adapted for use in children.
- 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_69c0085047dc8190af24e311edad3c07 |
completed | March 22, 2026, 3:18 p.m. |
| NER | Named-entity recognition | batch_69c035f99b788190b5b06d83b9499bfa |
completed | March 22, 2026, 6:33 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69c0b11b48d88190ba6cd5ade2f47a89 |
completed | March 23, 2026, 3:18 a.m. |
Created at: March 22, 2026, 3:57 p.m.