Triple
T22878617
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Directive 2004/24/EC |
E567395
|
entity |
| Predicate | alsoKnownAs |
P39
|
FINISHED |
| Object | Traditional Herbal Medicinal Products Directive |
—
|
NE NERFINISHED |
How this triple was built (3 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: Traditional Herbal Medicinal Products Directive | Statement: [Directive 2004/24/EC, alsoKnownAs, Traditional Herbal Medicinal Products Directive]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Traditional Herbal Medicinal Products Directive Context triple: [Directive 2004/24/EC, alsoKnownAs, Traditional Herbal Medicinal Products Directive]
-
A.
European Pharmacopoeia
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.
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.
-
C.
Community code for medicinal products for human use
The Community code for medicinal products for human use is a comprehensive European Union regulatory framework that harmonizes the authorization, supervision, and distribution of human medicines across EU member states.
-
D.
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.
-
E.
Therapeutic Products Act
The Therapeutic Products Act is a Swiss federal law that regulates the authorization, monitoring, and safe use of medicines and medical devices in Switzerland.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Traditional Herbal Medicinal Products Directive Target entity description: The Traditional Herbal Medicinal Products Directive is a European Union law that sets specific registration and safety requirements for traditional herbal medicines sold within the EU.
-
A.
European Pharmacopoeia
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.
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.
-
C.
Community code for medicinal products for human use
The Community code for medicinal products for human use is a comprehensive European Union regulatory framework that harmonizes the authorization, supervision, and distribution of human medicines across EU member states.
-
D.
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.
-
E.
Therapeutic Products Act
The Therapeutic Products Act is a Swiss federal law that regulates the authorization, monitoring, and safe use of medicines and medical devices in Switzerland.
- F. None of above. chosen
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_69e24589d8348190b96422d13a678bc1 |
completed | April 17, 2026, 2:36 p.m. |
| NER | Named-entity recognition | batch_69f17f5a26f4819086ede6d85a2ab2bf |
completed | April 29, 2026, 3:47 a.m. |
Created at: April 17, 2026, 3:39 p.m.