Triple

T22457973
Position Surface form Disambiguated ID Type / Status
Subject Swissmedic E555161 entity
Predicate appliesRegulation P1129 FINISHED
Object Therapeutic Products Act
The Therapeutic Products Act is a Swiss federal law that regulates the authorization, monitoring, and safe use of medicines and medical devices in Switzerland.
 E1538037 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: Therapeutic Products Act | Statement: [Swissmedic, appliesRegulation, Therapeutic Products Act]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Therapeutic Products Act
Context triple: [Swissmedic, appliesRegulation, Therapeutic Products Act]
  • A. Medicines Act 1968
    The Medicines Act 1968 is a key UK law that regulates the manufacture, licensing, distribution, and sale of medicinal products to ensure their safety, quality, and efficacy.
  • B. Controlled Drugs and Substances Act
    The Controlled Drugs and Substances Act is a Canadian federal law that regulates the possession, production, distribution, and sale of controlled drugs and substances, including associated criminal offences and penalties.
  • C. 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.
  • D. Pharmacy Act, 1948
    The Pharmacy Act, 1948 is an Indian law that regulates the profession and practice of pharmacy, including education standards and registration of pharmacists across the country.
  • E. Consumer Packaging and Labelling Act (except food)
    The Consumer Packaging and Labelling Act (except food) is a Canadian federal law that sets mandatory standards for accurate, clear, and non-deceptive labelling and packaging of most consumer products other than food.
  • 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: Therapeutic Products Act
Triple: [Swissmedic, appliesRegulation, Therapeutic Products Act]
Generated description
The Therapeutic Products Act is a Swiss federal law that regulates the authorization, monitoring, and safe use of medicines and medical devices in Switzerland.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07 
Target entity: Therapeutic Products Act
Target entity description: The Therapeutic Products Act is a Swiss federal law that regulates the authorization, monitoring, and safe use of medicines and medical devices in Switzerland.
  • A. Medicines Act 1968
    The Medicines Act 1968 is a key UK law that regulates the manufacture, licensing, distribution, and sale of medicinal products to ensure their safety, quality, and efficacy.
  • B. Controlled Drugs and Substances Act
    The Controlled Drugs and Substances Act is a Canadian federal law that regulates the possession, production, distribution, and sale of controlled drugs and substances, including associated criminal offences and penalties.
  • C. 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.
  • D. Pharmacy Act, 1948
    The Pharmacy Act, 1948 is an Indian law that regulates the profession and practice of pharmacy, including education standards and registration of pharmacists across the country.
  • E. Consumer Packaging and Labelling Act (except food)
    The Consumer Packaging and Labelling Act (except food) is a Canadian federal law that sets mandatory standards for accurate, clear, and non-deceptive labelling and packaging of most consumer products other than food.
  • 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_69e11e51fdec8190adfdf9f8a6362221 completed April 16, 2026, 5:37 p.m.
NER Named-entity recognition batch_69f15b7d00208190955a70e2c22d25a4 completed April 29, 2026, 1:14 a.m.
NED1 Entity disambiguation (via context triple) batch_6a0b0c7fc40081909f27eb081ac156f1 completed May 18, 2026, 12:56 p.m.
NEDg Description generation batch_6a0b0ddb116c8190b19f9a01abb737e6 completed May 18, 2026, 1:02 p.m.
NED2 Entity disambiguation (via description) batch_6a0b0e4402e481909210c5feff3fcddf completed May 18, 2026, 1:04 p.m.
Created at: April 16, 2026, 8:48 p.m.