Triple

T18750528
Position Surface form Disambiguated ID Type / Status
Subject MDR E458512 entity
Predicate alsoKnownAs P39 FINISHED
Object Medical Device Regulation NE NERFINISHED

How this triple was built (2 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: Medical Device Regulation | Statement: [MDR, alsoKnownAs, Medical Device Regulation]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Medical Device Regulation
Context triple: [MDR, alsoKnownAs, Medical Device Regulation]
  • 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. MedTech
    MedTech is Johnson & Johnson’s medical technology division, focused on developing and providing advanced devices and solutions for surgery, orthopedics, cardiovascular care, and other clinical specialties.
  • C. Innovation in Medical Technology
    "Innovation in Medical Technology" is a scholarly work examining how new medical technologies are developed, evaluated, and integrated into healthcare systems, and the implications this has for policy, costs, and patient outcomes.
  • D. Analytical, Diagnostic and Therapeutic Techniques and Equipment
    Analytical, Diagnostic and Therapeutic Techniques and Equipment is a broad medical subject category encompassing the tools, procedures, and methods used to detect, analyze, and treat health conditions.
  • E. Center for Devices and Radiological Health
    The Center for Devices and Radiological Health is the U.S. FDA division responsible for regulating medical devices and radiation-emitting products to ensure their safety and effectiveness.
  • F. None of above.
  • G. Unsure - the case is ambiguous/there is not enough information to decide.

Provenance (2 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_69d8d394dc308190b6725073f5db324c completed April 10, 2026, 10:40 a.m.
NER Named-entity recognition batch_69e579ec71cc8190bb6d3fa6cca6dc8c completed April 20, 2026, 12:57 a.m.
Created at: April 10, 2026, 11:51 a.m.