Matches in Nanopublications for { ?s ?p "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1011.RAqXBPCZl_jLigTCfFubI8HJqm215lEc28S842oeA9wt8130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011.RAqXBPCZl_jLigTCfFubI8HJqm215lEc28S842oeA9wt8130_provenance.
- NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833713.RA9mz5U6VxywN1pwR0RKc1J63OU_idQ6vsgdQWZGGDNC8130_provenance.
- NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- NP936943.RAn30COKO--0GMVqbqwz0g4_Ke_ppN0lOzlw6yDQtFDI4130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936943.RAn30COKO--0GMVqbqwz0g4_Ke_ppN0lOzlw6yDQtFDI4130_provenance.
- assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP667223.RAeXApqwv6yPuAiql-PZMivus7m6o692RxUutB42G1YaM130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667223.RAeXApqwv6yPuAiql-PZMivus7m6o692RxUutB42G1YaM130_provenance.
- NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818183.RAGzaLF_ih_4ZY7Fs_4VWgHWu1cP_x0J6Lv01sQqE0iN8130_provenance.
- NP5352.RA5hSDfxke2OGuYFfJ8cUx035YJbhxHQecOCguJRhhGGA130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5352.RA5hSDfxke2OGuYFfJ8cUx035YJbhxHQecOCguJRhhGGA130_provenance.
- NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667220.RALfNGpNgG11SyZrm61dv_Wjnd_zS0LTnmx9lXnqIW-fA130_provenance.