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GENE-CDS - Genomic Clinical Decision Support Ontology

The Genomic CDS ontology aims to unify several functionalities in a single resource, being: * A knowledge base for clinical pharmacogenomics/pharmacogenetics that can be used for question-answering (e.g., which SNPs are associated with this drug?) * A rule base for clinical decision support (e.g., inferring that a patient with a specific set of SNPs requires a lowered dose of warfarin and generating a CDS message that can be viewed by clinicians) * A tool for checking data consistency (e.g., highlighting which allele definitions in PharmGKB are overlapping, or which clinical decision support rules are matching the same group of patients)

Ontology metadata

Homepage http://samwald.info
Contactsamwald@gmx.at
Topicspreclinical and clinical studies, functional genomics, pharmacogenomics, map, genetic variation
SpeciesHuman
Class Count2265
Unsatisfiable classes0
dc:contributor
Contributors are those that engage in discussions in the context of the Genomic CDS ontology:
Bob Freimuth,
Michel Dumontier, 
Bob Powers, 
Simon Lin, 
Scott Marshall, 
Joanne Luciano, 
Richard Boyce, 
Eric Prud'Hommeaux
dc:creator
Matthias Samwald, http://samwald.info/
dc:license
Creative Commons 3.0 CC-by license
owl:versionInfo
0.8.0
rdfs:comment
If you want to contribute or report a bug, please write an e-mail to Matthias Samwald, samwald@gmx.at
rdfs:label
Pharmacogenomic Clinical Decision Support ontology ('Genomic CDS')
Date Download
Wed, 21 Nov 2012 00:00:00 GMT Download...

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