Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion> ?p ?o ?g. }
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- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion type Assertion NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_head.
- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion description "[Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_provenance.
- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion evidence source_evidence_literature NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_provenance.
- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion SIO_000772 17635637 NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_provenance.
- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion wasDerivedFrom befree-20150227 NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_provenance.
- NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_assertion wasGeneratedBy ECO_0000203 NP352812.RAvRDn6eLxXTFzncu9IMmVhmyPbIg3kxJhfC5RpDKXXwA130_provenance.