Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion description "[Although cases of adult patients with DCM caused by mutations of the genes encoding sarcomeric or cytoskeletal proteins of cardiomyocytes are infrequent in Japan, it may be advisable to screen older DCM patients for MYBPC3 mutations, and male patients with familial DCM for dystrophin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion evidence source_evidence_literature NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion SIO_000772 15671604 NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion wasDerivedFrom befree-2016 NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_assertion wasGeneratedBy ECO_0000203 NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.
- befree-2016 importedOn "2016-02-19" NP478043.RA-2rUee0G2-UoewzCPAqfhKOH5-Fy03rROWXhl6EzDlY130_provenance.