Triple

T21694398
Position Surface form Disambiguated ID Type / Status
Subject Centre for Drug Safety E535462 entity
Predicate collaboratesWith P37 FINISHED
Object Norwegian Medicines Agency 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: Norwegian Medicines Agency | Statement: [Centre for Drug Safety, collaboratesWith, Norwegian Medicines Agency]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Norwegian Medicines Agency
Context triple: [Centre for Drug Safety, collaboratesWith, Norwegian Medicines Agency]
  • A. Norwegian Medicines Agency chosen
    The Norwegian Medicines Agency is Norway’s national regulatory authority responsible for the approval, monitoring, and safe use of medicines and related health products.
  • B. Norwegian Directorate of Health
    The Norwegian Directorate of Health is a national government agency responsible for implementing health policy, issuing professional guidelines, and supporting the healthcare system in Norway.
  • C. Finnish Medicines Agency
    The Finnish Medicines Agency is Finland’s national authority responsible for regulating and supervising medicines and pharmaceutical safety.
  • D. Norwegian Institute of Public Health
    The Norwegian Institute of Public Health is Norway’s national public health agency responsible for disease surveillance, health research, and providing evidence-based advice to authorities and the public.
  • E. Norwegian Medicines Act
    The Norwegian Medicines Act is a key piece of Norwegian legislation that regulates the production, approval, distribution, and use of medicinal products to ensure their quality, safety, and proper control.
  • 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_69e0c46a6ee481908836e1420fb78c9b completed April 16, 2026, 11:13 a.m.
NER Named-entity recognition batch_69ef9b79336081909000ceaa86f6aed3 completed April 27, 2026, 5:23 p.m.
Created at: April 16, 2026, 6:45 p.m.