Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1258032.RA2HhG_d94XO7HGvVvxnZ_o2i1mcS2G_lsf7VCLUkeh1k#assertion> ?p ?o ?g. }
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- 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." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 23456229 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.