Triple
T23516985
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Central Drugs Standard Control Organisation |
E574393
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | drug regulatory agency |
C10842
|
CONCEPT FINISHED |
How this triple was built (1 step)
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.
CD
Concept disambiguation
gpt-5-mini-2025-08-07
Target class: drug regulatory agency Context triple: [Central Drugs Standard Control Organisation, instanceOf, drug regulatory agency]
-
A.
pharmacy regulator
A pharmacy regulator is an authority or organization responsible for overseeing, licensing, and enforcing standards for pharmacies and pharmacists to ensure the safe, ethical, and effective use of medications.
-
B.
drug control agency
chosen
A drug control agency is a governmental or intergovernmental body responsible for regulating, monitoring, and enforcing laws related to the production, distribution, prescription, and use of controlled substances to prevent abuse and ensure public safety.
-
C.
regulatory agency component
A regulatory agency component is a modular part of a regulatory body responsible for performing specific oversight, rulemaking, enforcement, or compliance functions within a defined domain.
-
D.
center of the U.S. Food and Drug Administration
The center of the U.S. Food and Drug Administration is the primary organizational unit within the FDA responsible for regulating and overseeing a specific category of products, such as drugs, biologics, or medical devices, to ensure their safety and effectiveness.
-
E.
U.S. Food and Drug Administration center
A U.S. Food and Drug Administration center is a specialized organizational unit within the FDA responsible for regulating and overseeing specific categories of products, such as drugs, biologics, medical devices, or food, to ensure their safety, effectiveness, and proper labeling.
- F. None of above.
Provenance (1 batch)
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_69e245bb3dcc8190ba9a2b35972b58d0 |
completed | April 17, 2026, 2:37 p.m. |
Created at: April 17, 2026, 6:08 p.m.