Triple
T34510917
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | U.S. Food and Drug Administration Office of Pediatric Therapeutics |
E886017
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | pediatric regulatory office |
C59217
|
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: pediatric regulatory office Context triple: [U.S. Food and Drug Administration Office of Pediatric Therapeutics, instanceOf, pediatric regulatory office]
-
A.
pharmaceutical regulatory agency
A pharmaceutical regulatory agency is a governmental or authoritative body responsible for evaluating, approving, and monitoring the safety, efficacy, quality, and marketing of medicinal products within its jurisdiction.
-
B.
child care regulatory agency
A child care regulatory agency is a governmental or authorized body responsible for setting, monitoring, and enforcing standards to ensure the safety, quality, and legal compliance of child care services.
-
C.
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.
-
D.
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.
-
E.
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.
- F. None of above. chosen
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_69f349ccc290819089d8e82698e53cb6 |
completed | April 30, 2026, 12:23 p.m. |
Created at: May 1, 2026, 2:01 a.m.