Triple
T2913024
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Integrated Award Environment |
E63727
|
entity |
| Predicate | replacedSystem |
P3618
|
FINISHED |
| Object | CFDA.gov |
E310832
|
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: CFDA.gov | Statement: [Integrated Award Environment, replacedSystem, CFDA.gov]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: CFDA.gov Context triple: [Integrated Award Environment, replacedSystem, CFDA.gov]
-
A.
CFDA.gov
chosen
CFDA.gov was the official U.S. government website that cataloged and provided detailed information on all federal financial assistance programs.
-
B.
Food and Drug Administration
The Food and Drug Administration is a U.S. federal agency responsible for protecting public health by regulating food, drugs, medical devices, and other consumer products.
-
C.
Office of Regulatory Affairs
The Office of Regulatory Affairs is the U.S. FDA’s primary field organization responsible for inspecting regulated products and manufacturers, enforcing compliance, and overseeing import operations to protect public health.
-
D.
Center for Biologics Evaluation and Research
The Center for Biologics Evaluation and Research is the U.S. regulatory body responsible for overseeing the safety, efficacy, and quality of biological products such as vaccines, blood products, and gene therapies.
-
E.
Center for Devices and Radiological Health
The Center for Devices and Radiological Health is the U.S. FDA division responsible for regulating medical devices and radiation-emitting products to ensure their safety and effectiveness.
- 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_69ab4c44ab448190b9411324e8a1fc1d |
completed | March 6, 2026, 9:51 p.m. |
| NER | Named-entity recognition | batch_69abe0ecaba48190a8e22c74a111fded |
completed | March 7, 2026, 8:25 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69b0865c719c8190aacafe236b02c844 |
completed | March 10, 2026, 9 p.m. |
Created at: March 6, 2026, 10:11 p.m.