Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_assertion description "[Differences were observed in the frequency of splice site and frame-shift mutations in the gene MYBPC3, which occurred more frequently (P< 0.02, P< 0.001, respectively) in HCM than in DCM, suggesting that cardiac myosin-binding protein C haploinsufficiency predisposes to hypertrophy rather than to dilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_assertion evidence source_evidence_literature NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_assertion SIO_000772 21750094 NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_assertion wasDerivedFrom befree-2016 NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_assertion wasGeneratedBy ECO_0000203 NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.
- befree-2016 importedOn "2016-02-19" NP909111.RAvKN1PXa-cTKhfhaqxyr5EVVRTsr9ab9g6jJXvPZALH0130_provenance.