Triple
T4617055
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | European Union medical device regulations |
E100892
|
entity |
| Predicate | hasCoreInstrument |
P26810
|
FINISHED |
| Object |
Regulation (EU) 2017/745 on medical devices
Regulation (EU) 2017/745 on medical devices is the main European Union legislative framework that sets comprehensive safety, performance, and market access requirements for medical devices placed on the EU market.
|
E100892
|
NE FINISHED |
How this triple was built (5 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: Regulation (EU) 2017/745 on medical devices | Statement: [European Union medical device regulations, hasCoreInstrument, Regulation (EU) 2017/745 on medical devices]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2017/745 on medical devices Context triple: [European Union medical device regulations, hasCoreInstrument, Regulation (EU) 2017/745 on medical devices]
-
A.
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.
-
B.
Regulation (EU) 2018/1727
Regulation (EU) 2018/1727 is the EU legal act that establishes and governs the functioning, mandate, and powers of Eurojust in supporting and coordinating cross-border criminal investigations and prosecutions among Member States.
-
C.
Regulation (EU) No 1151/2012
Regulation (EU) No 1151/2012 is a European Union law that establishes the quality schemes and protection framework for agricultural products and foodstuffs, including designations such as Protected Designation of Origin and Protected Geographical Indication.
-
D.
Regulation (EU) 2018/1725
Regulation (EU) 2018/1725 is the EU law that sets out data protection rules for EU institutions, bodies, offices and agencies, aligning them with the General Data Protection Regulation (GDPR).
-
E.
Regulation (EU) 2016/794
Regulation (EU) 2016/794 is an EU legal act that modernised and strengthened the mandate, structure, and operational framework of Europol as the Union’s law enforcement agency.
- 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: Regulation (EU) 2017/745 on medical devices Triple: [European Union medical device regulations, hasCoreInstrument, Regulation (EU) 2017/745 on medical devices]
Generated description
Regulation (EU) 2017/745 on medical devices is the main European Union legislative framework that sets comprehensive safety, performance, and market access requirements for medical devices placed on the EU market.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Regulation (EU) 2017/745 on medical devices Target entity description: Regulation (EU) 2017/745 on medical devices is the main European Union legislative framework that sets comprehensive safety, performance, and market access requirements for medical devices placed on the EU market.
-
A.
European Union medical device regulations
chosen
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.
-
B.
Regulation (EU) 2018/1727
Regulation (EU) 2018/1727 is the EU legal act that establishes and governs the functioning, mandate, and powers of Eurojust in supporting and coordinating cross-border criminal investigations and prosecutions among Member States.
-
C.
Regulation (EU) No 1151/2012
Regulation (EU) No 1151/2012 is a European Union law that establishes the quality schemes and protection framework for agricultural products and foodstuffs, including designations such as Protected Designation of Origin and Protected Geographical Indication.
-
D.
Regulation (EU) 2018/1725
Regulation (EU) 2018/1725 is the EU law that sets out data protection rules for EU institutions, bodies, offices and agencies, aligning them with the General Data Protection Regulation (GDPR).
-
E.
Regulation (EU) 2016/794
Regulation (EU) 2016/794 is an EU legal act that modernised and strengthened the mandate, structure, and operational framework of Europol as the Union’s law enforcement agency.
- F. None of above.
PD
Predicate disambiguation
gpt-5-mini-2025-08-07
Target predicate: hasCoreInstrument Context triple: [European Union medical device regulations, hasCoreInstrument, Regulation (EU) 2017/745 on medical devices]
-
A.
coreInstrument
chosen
Indicates that an instrument plays a central or primary role in performing an action or achieving an outcome.
-
B.
usesInstrument
Indicates that an agent performs an action by employing a specific instrument or tool as the means to carry it out.
-
C.
hasNotableInstrumentNamedAfter
Indicates that an entity has a notable musical instrument that is named after it.
-
D.
hasMusicalInstrument
Indicates that one entity possesses, uses, or is associated with a particular musical instrument.
-
E.
hasOrchestralFeature
Indicates that something includes, exhibits, or is characterized by a notable orchestral element or component.
- F. None of above.
Provenance (6 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_69bd43cf363c819087fd5ab441b4a3f4 |
completed | March 20, 2026, 12:55 p.m. |
| NER | Named-entity recognition | batch_69bd59e098c08190b769e76937dff700 |
completed | March 20, 2026, 2:29 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69bdfa8da23881909ba4a70e9697f260 |
completed | March 21, 2026, 1:55 a.m. |
| NEDg | Description generation | batch_69bdfc7b84108190af39c7780f702745 |
completed | March 21, 2026, 2:03 a.m. |
| NED2 | Entity disambiguation (via description) | batch_69bdfd3856b48190a44f49da5fde38f6 |
completed | March 21, 2026, 2:06 a.m. |
| PD | Predicate disambiguation | batch_69bd522fd5c48190ad2bffc0a5bc9061 |
completed | March 20, 2026, 1:57 p.m. |
Created at: March 20, 2026, 1:12 p.m.