Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_assertion description "[One candidate gene in the region, MYH7, which is mutated in cardiomyopathy and myosin storage myopathy, codes for the myosin heavy chain of type I skeletal muscle fibers and cardiac ventricles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_assertion evidence source_evidence_literature NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_assertion SIO_000772 15322983 NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_assertion wasDerivedFrom befree-2016 NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_assertion wasGeneratedBy ECO_0000203 NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.
- befree-2016 importedOn "2016-02-19" NP456838.RAch4loOvQBykAwVSvKiBHZK8lNUP3h3pXlVrpJKMGA-s130_provenance.