Triple

T6769628
Position Surface form Disambiguated ID Type / Status
Subject EU Tissues and Cells Directives E155010 entity
Predicate includes P1393 FINISHED
Object Directive 2006/17/EC
Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
E619864 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: Directive 2006/17/EC | Statement: [EU Tissues and Cells Directives, includes, Directive 2006/17/EC]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Directive 2006/17/EC
Context triple: [EU Tissues and Cells Directives, includes, Directive 2006/17/EC]
  • A. Directive 2004/23/EC
    Directive 2004/23/EC is a key European Union law that sets quality and safety standards for the donation, procurement, testing, processing, preservation, storage, and distribution of human tissues and cells for medical use.
  • B. Directive 2009/147/EC
    Directive 2009/147/EC is a key European Union law on the conservation of wild birds, forming one of the main legal pillars of the Natura 2000 protected areas network.
  • C. Directive 2004/24/EC
    Directive 2004/24/EC is a European Union law that created a simplified registration and regulatory framework for traditional herbal medicinal products across EU member states.
  • D. Directive 2006/86/EC
    Directive 2006/86/EC is a European Union legal act that sets detailed technical requirements for the traceability, notification of serious adverse reactions and events, and quality and safety standards for human tissues and cells used in medical treatments.
  • E. Directive 2001/82/EC
    Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
  • 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: Directive 2006/17/EC
Triple: [EU Tissues and Cells Directives, includes, Directive 2006/17/EC]
Generated description
Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Directive 2006/17/EC
Target entity description: Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
  • A. Directive 2004/23/EC
    Directive 2004/23/EC is a key European Union law that sets quality and safety standards for the donation, procurement, testing, processing, preservation, storage, and distribution of human tissues and cells for medical use.
  • B. Directive 2009/147/EC
    Directive 2009/147/EC is a key European Union law on the conservation of wild birds, forming one of the main legal pillars of the Natura 2000 protected areas network.
  • C. Directive 2004/24/EC
    Directive 2004/24/EC is a European Union law that created a simplified registration and regulatory framework for traditional herbal medicinal products across EU member states.
  • D. Directive 2006/86/EC
    Directive 2006/86/EC is a European Union legal act that sets detailed technical requirements for the traceability, notification of serious adverse reactions and events, and quality and safety standards for human tissues and cells used in medical treatments.
  • E. Directive 2001/82/EC
    Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
  • 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_69c68812ef7c819099369f51febb725c completed March 27, 2026, 1:37 p.m.
NER Named-entity recognition batch_69c6d232d1f08190bc30c0f24f28c475 completed March 27, 2026, 6:53 p.m.
NED1 Entity disambiguation (via context triple) batch_69c71a7da01c8190995885eeb4ba6253 completed March 28, 2026, 12:02 a.m.
NEDg Description generation batch_69c71b88b27c8190b803f0e9f6402c44 completed March 28, 2026, 12:06 a.m.
NED2 Entity disambiguation (via description) batch_69c71c91e08c81908be81efc2087464a completed March 28, 2026, 12:10 a.m.
Created at: March 27, 2026, 2:13 p.m.