Triple
T2664415
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Yellow Card Scheme |
E55600
|
entity |
| Predicate | operatedBy |
P86
|
FINISHED |
| Object | MHRA |
E10163
|
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: MHRA | Statement: [Yellow Card Scheme, operatedBy, MHRA]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: MHRA Context triple: [Yellow Card Scheme, operatedBy, MHRA]
-
A.
UK Medicines and Healthcare products Regulatory Agency
chosen
The UK Medicines and Healthcare products Regulatory Agency is the United Kingdom’s national authority responsible for regulating medicines, medical devices, and healthcare products to ensure their safety, quality, and effectiveness.
-
B.
Committee for Proprietary Medicinal Products
The Committee for Proprietary Medicinal Products was a former scientific committee of the European Union responsible for evaluating and issuing opinions on the quality, safety, and efficacy of human medicinal products before it was replaced by the European Medicines Agency’s current committee structure.
-
C.
Committee for Medicinal Products for Human Use
The Committee for Medicinal Products for Human Use is the European Medicines Agency’s expert body responsible for evaluating and providing scientific opinions on the safety, quality, and efficacy of medicines for human use in the European Union.
-
D.
European Medicines Agency
The European Medicines Agency is the European Union’s regulatory authority responsible for the scientific evaluation, supervision, and safety monitoring of medicines for human and veterinary use.
-
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_69ab49e54de48190be708cd1cf8be073 |
completed | March 6, 2026, 9:40 p.m. |
| NER | Named-entity recognition | batch_69abd96dba44819085c3e651afba7806 |
completed | March 7, 2026, 7:53 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69afa056f478819091f6751edfee0132 |
completed | March 10, 2026, 4:38 a.m. |
Created at: March 6, 2026, 9:54 p.m.