Triple

T18750407
Position Surface form Disambiguated ID Type / Status
Subject Good Manufacturing Practices E458509 entity
Predicate isRelatedTo P37 FINISHED
Object Good Clinical Practice — 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: Good Clinical Practice | Statement: [Good Manufacturing Practices, isRelatedTo, Good Clinical Practice]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: Good Clinical Practice
Context triple: [Good Manufacturing Practices, isRelatedTo, Good Clinical Practice]
  • A. ICH E6 Good Clinical Practice chosen
    ICH E6 Good Clinical Practice is an international ethical and scientific quality standard that governs the design, conduct, recording, and reporting of clinical trials involving human subjects.
  • B. Good Manufacturing Practices
    Good Manufacturing Practices are a set of regulatory and industry standards that ensure products are consistently produced and controlled to quality and safety requirements, particularly in sectors like food, pharmaceuticals, and cosmetics.
  • C. ICH E8 General Considerations for Clinical Trials
    ICH E8 General Considerations for Clinical Trials is an international guideline that outlines fundamental principles and quality considerations for the design, conduct, and evaluation of clinical studies across all phases of drug development.
  • D. ICH M3(R2) Nonclinical Safety Studies for the Conduct of Human Clinical Trials and Marketing Authorization for Pharmaceuticals
    ICH M3(R2) is an international guideline that harmonizes requirements for nonclinical safety studies needed to support the initiation and progression of human clinical trials and the marketing authorization of pharmaceuticals.
  • E. Best Current Practice
    Best Current Practice is a series of IETF documents that record community consensus on recommended methods, procedures, and guidelines for using and managing Internet technologies.
  • 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.