Triple

T1151211
Position Surface form Disambiguated ID Type / Status
Subject International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use E23680 entity
Predicate notableWork P4 FINISHED
Object ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals
ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals is an international regulatory guideline that outlines the nonclinical safety studies needed to support the development and approval of anticancer drugs in humans.
E131972 NE FINISHED

How this triple was built (4 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: ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals | Statement: [International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use, notableWork, ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals
Context triple: [International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use, notableWork, ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals]
  • A. Molecular Cancer Therapeutics
    Molecular Cancer Therapeutics is a peer-reviewed scientific journal focusing on the discovery, development, and clinical evaluation of novel cancer therapeutics.
  • B. Pharmacovigilance Risk Assessment Committee within the European Medicines Agency
    The Pharmacovigilance Risk Assessment Committee within the European Medicines Agency is an expert body responsible for evaluating and monitoring the safety of medicines across the European Union and providing recommendations on managing and communicating medicine-related risks.
  • C. Cancer Res
    Cancer Res is a leading peer-reviewed scientific journal that publishes research on the molecular and cellular biology, genetics, and treatment of cancer.
  • D. NCI-Designated Cancer Centers Program
    The NCI-Designated Cancer Centers Program is a U.S. network of leading academic and research institutions recognized for excellence in cancer research, treatment, and prevention.
  • E. National Institutes of Health intramural research program
    The National Institutes of Health intramural research program is a large, government-funded biomedical research enterprise in which NIH scientists conduct basic, translational, and clinical studies within NIH facilities.
  • 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: ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals
Triple: [International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use, notableWork, ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals]
Generated description
ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals is an international regulatory guideline that outlines the nonclinical safety studies needed to support the development and approval of anticancer drugs in humans.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals
Target entity description: ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals is an international regulatory guideline that outlines the nonclinical safety studies needed to support the development and approval of anticancer drugs in humans.
  • A. Molecular Cancer Therapeutics
    Molecular Cancer Therapeutics is a peer-reviewed scientific journal focusing on the discovery, development, and clinical evaluation of novel cancer therapeutics.
  • B. Pharmacovigilance Risk Assessment Committee within the European Medicines Agency
    The Pharmacovigilance Risk Assessment Committee within the European Medicines Agency is an expert body responsible for evaluating and monitoring the safety of medicines across the European Union and providing recommendations on managing and communicating medicine-related risks.
  • C. Cancer Res
    Cancer Res is a leading peer-reviewed scientific journal that publishes research on the molecular and cellular biology, genetics, and treatment of cancer.
  • D. NCI-Designated Cancer Centers Program
    The NCI-Designated Cancer Centers Program is a U.S. network of leading academic and research institutions recognized for excellence in cancer research, treatment, and prevention.
  • E. National Institutes of Health intramural research program
    The National Institutes of Health intramural research program is a large, government-funded biomedical research enterprise in which NIH scientists conduct basic, translational, and clinical studies within NIH facilities.
  • F. None of above. chosen

Provenance (5 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_69a493f0d32c8190ac74bad3c87f2641 completed March 1, 2026, 7:30 p.m.
NER Named-entity recognition batch_69a4bc744e7c81908f8612f2aad28600 completed March 1, 2026, 10:23 p.m.
NED1 Entity disambiguation (via context triple) batch_69ac5eb5d36c8190916a43a5f41df144 completed March 7, 2026, 5:21 p.m.
NEDg Description generation batch_69ac5f4756b08190b3dbaf64a9351836 completed March 7, 2026, 5:24 p.m.
NED2 Entity disambiguation (via description) batch_69ac600f78148190bd3109276f7b9e3a completed March 7, 2026, 5:27 p.m.
Created at: March 1, 2026, 7:44 p.m.