Triple
T15921505
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | CEP |
E386102
|
entity |
| Predicate | relatedTo |
P37
|
FINISHED |
| Object | European Pharmacopoeia |
E387634
|
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: European Pharmacopoeia | Statement: [CEP, relatedTo, European Pharmacopoeia]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: European Pharmacopoeia Context triple: [CEP, relatedTo, European Pharmacopoeia]
-
A.
European Pharmacopoeia
chosen
The European Pharmacopoeia is a legally binding reference work that sets quality standards for medicines and their ingredients across member states of the Council of Europe.
-
B.
Certificates of Suitability to the monographs of the European Pharmacopoeia
Certificates of Suitability to the monographs of the European Pharmacopoeia are official documents issued by the European Directorate for the Quality of Medicines & HealthCare (EDQM) confirming that a substance’s quality complies with the relevant European Pharmacopoeia monograph, thereby simplifying regulatory approval for medicines across Europe.
-
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.
European Directorate for the Quality of Medicines & HealthCare
The European Directorate for the Quality of Medicines & HealthCare is a Council of Europe body responsible for developing quality standards and guidance to ensure the safety and efficacy of medicines and improve healthcare across member states.
-
E.
Committee for Herbal Medicinal Products
The Committee for Herbal Medicinal Products is a scientific body within the European Medicines Agency that evaluates and provides guidance on the safety and efficacy of herbal medicines in the European Union.
- 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_69d86da686e4819097cbf3b1fc2d881d |
completed | April 10, 2026, 3:25 a.m. |
| NER | Named-entity recognition | batch_69e156825b1881908477ec93cc7b5f02 |
completed | April 16, 2026, 9:37 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69ffbe7055a48190b0f426f3e3c22f9d |
completed | May 9, 2026, 11:08 p.m. |
Created at: April 10, 2026, 4:52 a.m.