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.