Triple
T22404609
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Regulation (EU) No 536/2014 |
E553848
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | clinical trials regulation |
C31860
|
CONCEPT FINISHED |
How this triple was built (1 step)
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.
CD
Concept disambiguation
gpt-5-mini-2025-08-07
Target class: clinical trials regulation Context triple: [Regulation (EU) No 536/2014, instanceOf, clinical trials regulation]
-
A.
medical device regulation system
A medical device regulation system is a framework of processes, rules, and oversight mechanisms that govern the evaluation, approval, monitoring, and post-market surveillance of medical devices to ensure their safety, effectiveness, and compliance with regulatory standards.
-
B.
pharmaceutical law
Pharmaceutical law is the body of legal rules and regulations governing the research, development, approval, manufacturing, marketing, distribution, and use of drugs and medical products to ensure their safety, efficacy, and ethical oversight.
-
C.
clinical study
A clinical study is a structured research investigation involving human participants designed to evaluate the safety, efficacy, or outcomes of medical interventions, treatments, or health-related practices under predefined protocols.
-
D.
regulations
chosen
Regulations are authoritative rules or directives established by a governing body to control, manage, or guide behaviors and processes within a specific domain.
-
E.
medical research collaboration
A medical research collaboration is a coordinated partnership among researchers, clinicians, institutions, and sometimes industry or patient groups to jointly design, conduct, and analyze studies that advance medical knowledge and improve health outcomes.
- F. None of above.
Provenance (1 batch)
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_69e11e4da7048190b4387d422a9a0de5 |
completed | April 16, 2026, 5:37 p.m. |
Created at: April 16, 2026, 8:46 p.m.