Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion> ?p ?o ?g. }
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- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion type Assertion NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_head.
- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion description "[Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and cardiomyopathy, and genetically by mutations in the lamin A/C gene on 1q21.2-q21.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_provenance.
- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion evidence source_evidence_literature NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_provenance.
- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion SIO_000772 10908904 NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_provenance.
- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion wasDerivedFrom befree-20140225 NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_provenance.
- NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_assertion wasGeneratedBy ECO_0000203 NP761288.RAxBPYSUeOrchhejOmhc19d7zXx_CKpr3HeZQWK3ddrMU130_provenance.