Triple
T23958509
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Risk Assessment Framework for foundation trusts |
E603860
|
entity |
| Predicate | instanceOf |
P0
|
FINISHED |
| Object | NHS regulatory system |
C21060
|
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: NHS regulatory system Context triple: [Risk Assessment Framework for foundation trusts, instanceOf, NHS regulatory system]
-
A.
NHS indemnity scheme
The NHS indemnity scheme is a government-backed arrangement that provides legal and financial protection to NHS staff and organisations against claims arising from clinical negligence and certain non-clinical incidents in the course of their work.
-
B.
component of Integrated Care System in England
A component of an Integrated Care System in England is an organizational or functional unit (such as NHS providers, local authorities, or voluntary sector partners) that collaborates to plan, fund, and deliver coordinated health and care services for a defined population.
-
C.
NHS document
chosen
An NHS document is an official record or communication produced by the National Health Service that contains healthcare-related information, guidance, or data for patients, staff, or partner organizations.
-
D.
health systems research organisation
A health systems research organisation is an entity that systematically studies how health services are organized, financed, delivered, and governed to generate evidence that improves the performance, equity, and resilience of health systems.
-
E.
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.
- 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_69e2954222288190a7323554d0cca8d7 |
completed | April 17, 2026, 8:17 p.m. |
Created at: April 17, 2026, 9:22 p.m.