Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion> ?p ?o ?g. }
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- NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion type Assertion NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_head.
- NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion wasGeneratedBy ECO_0000203 NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_provenance.
- NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion wasDerivedFrom befree-20150227 NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_provenance.
- NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion SIO_000772 16550584 NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_provenance.
- NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion evidence source_evidence_literature NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_provenance.
- NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and DFNB12, whereas null alleles cause the majority of Usher 1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936895.RAKQ9S_f93ofoOVnUuAPYE0RjsUdDDvcmxR0yeA6BlImI130_provenance.