Triple
T5689007
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | FDA traditional approval |
E125382
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | FDA marketing authorization pathway |
C3993
|
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: FDA marketing authorization pathway Context triple: [FDA traditional approval, instanceOf, FDA marketing authorization pathway]
-
A.
regulatory filing
chosen
A regulatory filing is an official document or set of documents submitted to a government or regulatory authority to report required information, demonstrate compliance, or request approval related to an organization’s activities.
-
B.
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.
-
C.
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.
-
D.
pharmaceutical drug
A pharmaceutical drug is a chemically defined substance or combination of substances administered to diagnose, treat, prevent, or alleviate disease or medical conditions in humans or animals.
-
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_69c0082bb19c8190823a4facd3cba79b |
completed | March 22, 2026, 3:18 p.m. |
Created at: March 22, 2026, 3:44 p.m.