Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion type Assertion NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_head.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_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." NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion evidence source_evidence_literature NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion SIO_000772 10974018 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion wasDerivedFrom befree-2016 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion wasGeneratedBy ECO_0000203 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.