Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_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." NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_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." NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_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." NP936923.RAbUUZQMZzFQfslThX7m73OoI4zqxfqkdvld-ghllRmgg130_provenance.
- 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." provenance.
- NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_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." NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_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." NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_provenance.
- 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.
- 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." provenance.
- 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.