Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion description "[Two genes have been identified for the X-linked forms (dystrophin and tafazzin), whereas three other genes (actin, lamin A/C, and desmin) cause autosomal dominant DCM; seven other loci for autosomal dominant DCM have been mapped but the genes have not been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion evidence source_evidence_literature NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion SIO_000772 10974018 NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion wasDerivedFrom befree-20150227 NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion wasGeneratedBy ECO_0000203 NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_provenance.