Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion> ?p ?o ?g. }
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- NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion type Assertion NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_head.
- NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion description "[Mutations of lamin A/C (LMNA) cause a wide range of human disorders, including progeria, lipodystrophy, neuropathies and autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_provenance.
- NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion evidence source_evidence_literature NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_provenance.
- NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion SIO_000772 16478798 NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_provenance.
- NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion wasDerivedFrom befree-2016 NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_provenance.
- NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_assertion wasGeneratedBy ECO_0000203 NP535925.RA9lVcnOyPW2Gm0p0IvUodq90HOD3L1ALBPhWwDcDLd4M130_provenance.