Triple

T1339573
Position Surface form Disambiguated ID Type / Status
Subject Human Tissue Authority E28433 entity
Predicate hasLegalBasis P125 FINISHED
Object EU Tissues and Cells Directives
The EU Tissues and Cells Directives are a set of European Union laws that harmonize standards for the donation, testing, processing, storage, and distribution of human tissues and cells to ensure high levels of quality and safety across member states.
E155010 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: EU Tissues and Cells Directives | Statement: [Human Tissue Authority, hasLegalBasis, EU Tissues and Cells Directives]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: EU Tissues and Cells Directives
Context triple: [Human Tissue Authority, hasLegalBasis, EU Tissues and Cells Directives]
  • A. Human Tissue Authority
    The Human Tissue Authority is a UK regulatory body responsible for licensing and overseeing the removal, storage, use, and disposal of human bodies, organs, and tissue for purposes such as research, transplantation, and education.
  • B. NHS Blood and Transplant
    NHS Blood and Transplant is a UK special health authority responsible for providing a safe and reliable supply of blood, organs, and associated services to the National Health Service.
  • C. European Union medical device regulations
    European Union medical device regulations are a comprehensive set of legal and technical requirements governing the safety, performance, quality management, and market approval of medical devices within EU member states.
  • D. Cambridge Blood and Stem Cell Biobank
    The Cambridge Blood and Stem Cell Biobank is a major research facility that collects, processes, and stores human blood and stem cell samples to support biomedical and translational research.
  • E. Committee for Advanced Therapies
    The Committee for Advanced Therapies is a scientific body within the European Medicines Agency responsible for evaluating and providing expert opinions on advanced therapy medicinal products such as gene, cell, and tissue-engineered therapies.
  • 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: EU Tissues and Cells Directives
Triple: [Human Tissue Authority, hasLegalBasis, EU Tissues and Cells Directives]
Generated description
The EU Tissues and Cells Directives are a set of European Union laws that harmonize standards for the donation, testing, processing, storage, and distribution of human tissues and cells to ensure high levels of quality and safety across member states.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: EU Tissues and Cells Directives
Target entity description: The EU Tissues and Cells Directives are a set of European Union laws that harmonize standards for the donation, testing, processing, storage, and distribution of human tissues and cells to ensure high levels of quality and safety across member states.
  • A. Human Tissue Authority
    The Human Tissue Authority is a UK regulatory body responsible for licensing and overseeing the removal, storage, use, and disposal of human bodies, organs, and tissue for purposes such as research, transplantation, and education.
  • B. NHS Blood and Transplant
    NHS Blood and Transplant is a UK special health authority responsible for providing a safe and reliable supply of blood, organs, and associated services to the National Health Service.
  • C. European Union medical device regulations
    European Union medical device regulations are a comprehensive set of legal and technical requirements governing the safety, performance, quality management, and market approval of medical devices within EU member states.
  • D. Cambridge Blood and Stem Cell Biobank
    The Cambridge Blood and Stem Cell Biobank is a major research facility that collects, processes, and stores human blood and stem cell samples to support biomedical and translational research.
  • E. Committee for Advanced Therapies
    The Committee for Advanced Therapies is a scientific body within the European Medicines Agency responsible for evaluating and providing expert opinions on advanced therapy medicinal products such as gene, cell, and tissue-engineered therapies.
  • 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_69a49854eb3481908c7d56b2e449a290 completed March 1, 2026, 7:49 p.m.
NER Named-entity recognition batch_69a4c21303c881908fef0b32831222fe completed March 1, 2026, 10:47 p.m.
NED1 Entity disambiguation (via context triple) batch_69acc6305c988190830dd535726c6338 completed March 8, 2026, 12:43 a.m.
NEDg Description generation batch_69acc91793688190a223365d50498cc7 completed March 8, 2026, 12:55 a.m.
NED2 Entity disambiguation (via description) batch_69acc9b8c86c8190bc3526b85604884d completed March 8, 2026, 12:58 a.m.
Created at: March 1, 2026, 7:56 p.m.