Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion> ?p ?o ?g. }
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- NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion type Assertion NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_head.
- NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion description "[The more common X-linked recessive form of EDMD is caused by mutations in either EMD (encoding emerin) or FHL1 (encoding four and a half LIM domains 1), while mutations in LMNA (encoding lamin A/C), SYNE1 (encoding nesprin-1) and SYNE2 (encoding nesprin-2) lead to autosomal dominant forms of the condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_provenance.
- NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion evidence source_evidence_literature NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_provenance.
- NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion SIO_000772 23456229 NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_provenance.
- NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion wasDerivedFrom befree-20150227 NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_provenance.
- NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_assertion wasGeneratedBy ECO_0000203 NP537691.RAVOmzwIaVVsOgAWAkitf0TMrvafN0SrFWnPKDqrOXF9M130_provenance.