Triple
T15587413
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | FDHA |
E374657
|
entity |
| Predicate | oversees |
P46
|
FINISHED |
| Object | Swissmedic |
E555161
|
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: Swissmedic | Statement: [FDHA, oversees, Swissmedic]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Swissmedic Context triple: [FDHA, oversees, Swissmedic]
-
A.
Swissmedic
chosen
Swissmedic is the Swiss agency responsible for the authorization and supervision of therapeutic products, including medicines and medical devices, in Switzerland.
-
B.
Federal Institute for Drugs and Medical Devices
The Federal Institute for Drugs and Medical Devices is Germany’s central regulatory authority responsible for the authorization, safety monitoring, and risk assessment of pharmaceuticals and medical devices.
-
C.
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.
-
D.
European Union Drugs Agency
The European Union Drugs Agency is the EU’s central body responsible for providing scientific analysis, monitoring, and policy support on drugs and drug addiction across member states.
-
E.
European medicines regulatory authorities
European medicines regulatory authorities are national and regional agencies in Europe responsible for evaluating, authorizing, and monitoring the safety, quality, and efficacy of medicinal products.
- 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_69d85cce25008190b13b52745fbd719b |
completed | April 10, 2026, 2:13 a.m. |
| NER | Named-entity recognition | batch_69e04e4900408190aadb48b001db4169 |
completed | April 16, 2026, 2:49 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69ff4c53617c8190b4367eee351dc025 |
completed | May 9, 2026, 3:01 p.m. |
Created at: April 10, 2026, 4:11 a.m.