Triple

T2913016
Position Surface form Disambiguated ID Type / Status
Subject Integrated Award Environment E63727 entity
Predicate includesSystem P1393 FINISHED
Object CFDA.gov
CFDA.gov was the official U.S. government website that cataloged and provided detailed information on all federal financial assistance programs.
E310832 NE FINISHED

How this triple was built (4 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, includesSystem, CFDA.gov]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: CFDA.gov
Context triple: [Integrated Award Environment, includesSystem, CFDA.gov]
  • A. 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.
  • B. 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.
  • C. 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.
  • D. 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.
  • E. Federal Food, Drug, and Cosmetic Act
    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.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NEDg Description generation gpt-5.1
Instruction
Generate a one-sentence description of the target entity. 
You are given a context triple in the form (subject, predicate, object), where the object is the target entity. 
# Instructions
Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. 
Avoid repeating the information from the triple, unless really essential.
# Response Format
Return only the sentence: "Description: [one-sentence description of the target entity]"
Input
Entity: CFDA.gov
Triple: [Integrated Award Environment, includesSystem, CFDA.gov]
Generated description
CFDA.gov was the official U.S. government website that cataloged and provided detailed information on all federal financial assistance programs.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: CFDA.gov
Target entity description: CFDA.gov was the official U.S. government website that cataloged and provided detailed information on all federal financial assistance programs.
  • A. 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.
  • B. 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.
  • C. 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.
  • D. 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.
  • E. Federal Food, Drug, and Cosmetic Act
    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.
  • F. None of above. chosen

Provenance (5 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_69b056249b5c8190b388088bf047616f completed March 10, 2026, 5:34 p.m.
NEDg Description generation batch_69b06434bef48190848d8ab1aa59937c completed March 10, 2026, 6:34 p.m.
NED2 Entity disambiguation (via description) batch_69b064a3b41481909214a09eae0b092b completed March 10, 2026, 6:36 p.m.
Created at: March 6, 2026, 10:11 p.m.