Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_assertion> ?p ?o ?g. }
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- NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_assertion type Assertion NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_head.
- NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_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." NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_provenance.
- NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_assertion evidence source_evidence_literature NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_provenance.
- NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_assertion SIO_000772 11090341 NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_provenance.
- NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_assertion wasDerivedFrom befree-20150227 NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_provenance.
- NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_assertion wasGeneratedBy ECO_0000203 NP936905.RA249P53rPfAAlWv-wZIIUmGeSJfLmC5kRq1aKQxAiXXw130_provenance.