Matches in Nanopublications for { ?s ?p "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP147356.RAZthW3540PLU6yj_G5A7K6N2whSse19A3EYT9G_XRiSU130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147356.RAZthW3540PLU6yj_G5A7K6N2whSse19A3EYT9G_XRiSU130_provenance.
- NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153199.RAR6utspZgctmIGk1gnAS0LMUo9U5NLsq7U09hEJVmWtM130_provenance.
- NP210490.RA5KnTpbEcVR6ejQ5b6nz-pm5tBY-uwcZUgn4igdjV-7M130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210490.RA5KnTpbEcVR6ejQ5b6nz-pm5tBY-uwcZUgn4igdjV-7M130_provenance.
- NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_provenance.
- NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_provenance.
- assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and nonsyndromic prelingual hearing loss (DFNB12), whereas null alleles cause the majority of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216204.RAuqljnh-iW-7cYEcmqeWumSTYN6i5uX18UNCYjCf_VQQ130_provenance.