Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion> ?p ?o ?g. }
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- NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion type Assertion NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_head.
- NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion description "[Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_provenance.
- NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion evidence source_evidence_literature NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_provenance.
- NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion SIO_000772 11090341 NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_provenance.
- NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion wasDerivedFrom befree-2016 NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_provenance.
- NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_assertion wasGeneratedBy ECO_0000203 NP301122.RAeCnC1Oai-qex9Gq1VczgHgEJvclaMZJxW3WQLiG_rgA130_provenance.