Triple

T3148706
Position Surface form Disambiguated ID Type / Status
Subject Controlled Substances Act E65823 entity
Predicate relatedTo P37 FINISHED
Object Federal Analog Act
The Federal Analog Act is a U.S. drug law that allows substances substantially similar to already controlled drugs to be treated as illegal controlled substances when intended for human consumption.
E331256 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: Federal Analog Act | Statement: [Controlled Substances Act, relatedTo, Federal Analog Act]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Federal Analog Act
Context triple: [Controlled Substances Act, relatedTo, Federal Analog Act]
  • A. FDC Act
    The FDC Act is a key United States law that authorizes the Food and Drug Administration to regulate the safety, efficacy, and labeling of food, drugs, cosmetics, and certain medical devices.
  • B. Federal Register Act
    The Federal Register Act is a United States law that established the Federal Register system for officially publishing government rules, regulations, and notices.
  • C. Federal Trade Commission Act provisions
    The Federal Trade Commission Act provisions are U.S. federal laws that establish and empower the Federal Trade Commission to prevent unfair or deceptive business practices and promote consumer protection and fair competition.
  • D. 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.
  • E. 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.
  • 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: Federal Analog Act
Triple: [Controlled Substances Act, relatedTo, Federal Analog Act]
Generated description
The Federal Analog Act is a U.S. drug law that allows substances substantially similar to already controlled drugs to be treated as illegal controlled substances when intended for human consumption.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Federal Analog Act
Target entity description: The Federal Analog Act is a U.S. drug law that allows substances substantially similar to already controlled drugs to be treated as illegal controlled substances when intended for human consumption.
  • A. FDC Act
    The FDC Act is a key United States law that authorizes the Food and Drug Administration to regulate the safety, efficacy, and labeling of food, drugs, cosmetics, and certain medical devices.
  • B. Federal Register Act
    The Federal Register Act is a United States law that established the Federal Register system for officially publishing government rules, regulations, and notices.
  • C. Federal Trade Commission Act provisions
    The Federal Trade Commission Act provisions are U.S. federal laws that establish and empower the Federal Trade Commission to prevent unfair or deceptive business practices and promote consumer protection and fair competition.
  • D. 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.
  • E. 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.
  • 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_69ad8584485081909ed529e890cadc4a completed March 8, 2026, 2:19 p.m.
NER Named-entity recognition batch_69ada5be30fc819097edb620c65055d5 completed March 8, 2026, 4:37 p.m.
NED1 Entity disambiguation (via context triple) batch_69b224f94f3881909a277c45c9add0f5 completed March 12, 2026, 2:29 a.m.
NEDg Description generation batch_69b225b27e1c8190a3df0d4692ee66c6 completed March 12, 2026, 2:32 a.m.
NED2 Entity disambiguation (via description) batch_69b226339e4881908690f7ea7a7bd50c completed March 12, 2026, 2:34 a.m.
Created at: March 8, 2026, 3:05 p.m.