Triple
T7110739
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | FDC Act |
E165700
|
entity |
| Predicate | abbreviation |
P43
|
FINISHED |
| Object | FD&C Act |
E31160
|
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: FD&C Act | Statement: [FDC Act, abbreviation, FD&C Act]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: FD&C Act Context triple: [FDC Act, abbreviation, FD&C Act]
-
A.
Federal Food, Drug, and Cosmetic Act
chosen
The Federal Food, Drug, and Cosmetic Act is a key U.S. law that authorizes the Food and Drug Administration to regulate the safety, labeling, and marketing of food, drugs, medical devices, and cosmetics.
-
B.
Kefauver–Harris Drug Amendments of 1962
The Kefauver–Harris Drug Amendments of 1962 are U.S. federal regulations that strengthened drug safety and efficacy requirements, mandating proof of effectiveness and stricter oversight of pharmaceutical marketing and manufacturing.
-
C.
Pure Food and Drug Act of 1906
The Pure Food and Drug Act of 1906 was a landmark U.S. federal law that laid the foundation for modern consumer protection by prohibiting the manufacture and sale of adulterated or misbranded foods and drugs and leading to the creation of federal regulatory oversight.
-
D.
Controlled Substances Act
The Controlled Substances Act is a U.S. federal law that regulates the manufacture, distribution, and possession of certain drugs by classifying them into schedules based on their medical use and potential for abuse.
-
E.
Poison Prevention Packaging Act
The Poison Prevention Packaging Act is a U.S. federal law that requires child-resistant packaging for certain household substances to reduce the risk of accidental poisoning in children.
- 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_69c6888120f081908f8f01b201dc4a4c |
completed | March 27, 2026, 1:39 p.m. |
| NER | Named-entity recognition | batch_69c6e5be09d881909988b5382ffa20ed |
completed | March 27, 2026, 8:17 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69c7a325a07c81909bd9a8f5d4461fb9 |
completed | March 28, 2026, 9:45 a.m. |
Created at: March 27, 2026, 2:43 p.m.