Triple
T17056550
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | FDA field laboratories |
E413835
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | regulatory science facility |
C14386
|
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: regulatory science facility Context triple: [FDA field laboratories, instanceOf, regulatory science facility]
-
A.
research facility
A research facility is a specialized institution equipped with laboratories, instruments, and resources where scientists and experts systematically investigate, experiment, and develop new knowledge or technologies.
-
B.
National Science Foundation facility
A National Science Foundation facility is a research infrastructure, laboratory, observatory, or center funded or supported by the NSF to enable and advance scientific discovery and education across diverse disciplines.
-
C.
U.S. Food and Drug Administration center
chosen
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.
-
D.
research facility area
A research facility area is a designated space within or associated with a research institution where scientific, technical, or experimental activities are conducted, supported, or managed.
-
E.
medical device regulation system
A medical device regulation system is a framework of processes, rules, and oversight mechanisms that govern the evaluation, approval, monitoring, and post-market surveillance of medical devices to ensure their safety, effectiveness, and compliance with regulatory standards.
- 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_69d886cde3d481908d4d01ba88ba7eb7 |
completed | April 10, 2026, 5:12 a.m. |
Created at: April 10, 2026, 5:34 a.m.