Show simple item record

dc.contributor.authorSamwald, Matthias
dc.contributor.authorFreimuth, Robert
dc.contributor.authorLuciano, Joanne
dc.contributor.authorLin, Simon
dc.contributor.authorPowers, Robert
dc.contributor.authorMarshall, M.
dc.contributor.authorAdlassnig, Klaus-Peter
dc.contributor.authorDumontier, Michel
dc.contributor.authorBoyce, Richard
dc.date.accessioned2022-02-18T02:36:54Z
dc.date.available2022-02-18T02:36:54Z
dc.date.issued2013-08-20
dc.identifier.other128
dc.identifier.urihttp://archive.tw.rpi.edu/media/latest/Medinfo2013_JSL.pdf
dc.identifier.urihttps://hdl.handle.net/20.500.13015/4530
dc.description.abstractGenetic testing for personalizing pharmacotherapy is bound to become an important part of clinical routine. To address associated issues with data management and quality, we are creating a semantic knowledge base for clinical pharmaco- genetics. The knowledge base is made up of three components: an expressive ontology formalized in the Web Ontology Lan- guage (OWL 2 DL), a Resource Description Framework (RDF) model for capturing detailed results of manual annota- tion of pharmacogenomic information in drug product labels, and an RDF conversion of relevant biomedical datasets. Our work goes beyond the state of the art in that it makes both automated reasoning as well as query answering as simple as possible, and the reasoning capabilities go beyond the capa- bilities of previously described ontologies.
dc.relation.urihttps://tw.rpi.edu/project/SEMMDD
dc.subjectSemantically Enabled Modeling of Major Depressive Disorder
dc.titleAn RDF/OWL knowledge base for query answering and decision support in clinical pharmacogenetics


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record