Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion type Assertion NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_head.
- NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion wasGeneratedBy ECO_0000218 NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_provenance.
- NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion wasDerivedFrom uniprot-20130724 NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_provenance.
- NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion SIO_000772 11792809 NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_provenance.
- NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion evidence source_evidence_curated NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_provenance.
- NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy is caused by mutations in the LMNA gene, which encodes lamin A and lamin C. Mutations in this gene also give rise to limb girdle muscular dystrophy type 1B, dilated cardiomyopathy with atrioventricular conduction defect and Dunnigan-type partial lipodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3809.RAe5zycuJzn1PARqzhCrut3T53XmWvYj3GBTEO6QHX3bo130_provenance.