Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_assertion description "[Tenascin-X deficiency causes a clinically distinct, recessive form of the Ehlers-Danlos syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_assertion evidence source_evidence_literature NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_assertion SIO_000772 11642233 NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_assertion wasDerivedFrom befree-20140225 NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_assertion wasGeneratedBy ECO_0000203 NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP447590.RAd26nPKHxr3tsVhLYxf-DJmFlDi2EMLq77urAV0dmn0c130_provenance.