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- source_evidence_literature type ECO_0000212 NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_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." NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_assertion evidence source_evidence_literature NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_assertion SIO_000772 15322983 NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_assertion wasDerivedFrom befree-20140225 NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_assertion wasGeneratedBy ECO_0000203 NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.
- befree-20140225 importedOn "2014-02-25" NP346363.RASpX9qxCgxn19beoL3ePoV0-AmsiSCJVLJ-ZFyunNWss130_provenance.