Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion> ?p ?o ?g. }
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- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion type Assertion NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_head.
- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_provenance.
- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion evidence source_evidence_literature NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_provenance.
- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion SIO_000772 12687499 NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_provenance.
- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion wasDerivedFrom befree-20140225 NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_provenance.
- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion wasGeneratedBy ECO_0000203 NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_provenance.