Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion> ?p ?o ?g. }
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- NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_assertion type Assertion NP723627.RAASwRpPjYiZ58Wx73OB7y5rt8RWbaHpgIKl7nYqqd_CM130_head.
- 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.