Triple

T22965330
Position Surface form Disambiguated ID Type / Status
Subject European Union animal research directives E571025 entity
Predicate supports P516 FINISHED
Object EU reference laboratories for alternatives to animal testing NE NERFINISHED

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: EU reference laboratories for alternatives to animal testing | Statement: [European Union animal research directives, supports, EU reference laboratories for alternatives to animal testing]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: EU reference laboratories for alternatives to animal testing
Context triple: [European Union animal research directives, supports, EU reference laboratories for alternatives to animal testing]
  • A. European Union animal research directives
    European Union animal research directives are a set of EU-wide legal standards that govern the ethical treatment, housing, and use of animals in scientific research, emphasizing welfare, reduction of animal use, and strict oversight.
  • B. Experimental Toxicology and ZEBET
    Experimental Toxicology and ZEBET is a specialized section of Germany’s Federal Institute for Risk Assessment focused on experimental toxicology and the development and promotion of alternative methods to animal testing.
  • C. ICH S5 Reproductive Toxicity Testing Guidelines
    The ICH S5 Reproductive Toxicity Testing Guidelines are international standards that outline how to evaluate the potential effects of pharmaceuticals on fertility, embryo-fetal development, and pre- and postnatal development to support safe drug use in humans.
  • D. Public Health Service Policy on Humane Care and Use of Laboratory Animals
    The Public Health Service Policy on Humane Care and Use of Laboratory Animals is a U.S. federal framework that sets ethical and welfare standards for the housing, care, and use of animals in research funded or conducted by Public Health Service agencies.
  • E. European Union reference laboratories chosen
    European Union reference laboratories are specialized scientific institutions designated by the EU to provide expert analysis, standardization, and guidance on testing methods to ensure high and harmonized standards in areas such as animal health, food safety, and public health across member states.
  • F. None of above.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

Provenance (2 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_69e245b2c6548190a0e4c7f2f7df2d48 completed April 17, 2026, 2:37 p.m.
NER Named-entity recognition batch_69f1822e542c8190a865f18e64fc0768 completed April 29, 2026, 3:59 a.m.
Created at: April 17, 2026, 3:47 p.m.