Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion> ?p ?o ?g. }
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- NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion type Assertion NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_head.
- NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion description "[Phenotype in GJB2-associated hearing loss is correlated with genotype, with truncating mutations giving rise to more severe hearing loss. Progression of hearing loss is not uncommon, especially in association with the p.V37I allele. These results suggest ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_provenance.
- NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion evidence source_evidence_literature NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_provenance.
- NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion SIO_000772 20154630 NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_provenance.
- NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion wasDerivedFrom gad-20150221 NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_provenance.
- NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_assertion wasGeneratedBy ECO_0000203 NP51514.RAnWVOEiMIxmzDRBoib8G-bHAjU9Oklgcn4ruE1NdQ9eE130_provenance.