Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion> ?p ?o ?g. }
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- NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion type Assertion NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_head.
- NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion description "[Malignant mutation in the lamin A/C gene causing progressive conduction system disease and early sudden death in a family with mild form of limb-girdle muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_provenance.
- NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion evidence source_evidence_literature NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_provenance.
- NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion SIO_000772 17605093 NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_provenance.
- NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion wasDerivedFrom befree-2016 NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_provenance.
- NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_assertion wasGeneratedBy ECO_0000203 NP618069.RA3dXeqdL4tzRdiXsRn2a9sLsoYmE9uN_X8euDz7oFuT4130_provenance.