Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion description "[Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion evidence source_evidence_literature NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion SIO_000772 19412328 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion wasDerivedFrom gad-20130706 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_assertion wasGeneratedBy ECO_0000203 NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.
- gad-20130706 importedOn "2013-07-06" NP81920.RA47JmoO5hhoE_M4Um-SrydvebAaLC4Pc5o7dFTuMRRGw130_provenance.