Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion type Assertion NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_head.
- NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion wasGeneratedBy ECO_0000203 NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_provenance.
- NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion wasDerivedFrom lhgdn-20090331 NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_provenance.
- NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion SIO_000772 16550584 NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_provenance.
- NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_assertion evidence source_evidence_literature NP216203.RAwI15l3-FHAlbLoSu-9g3rmC6omdFLZYnqEcsUbBbeBQ130_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.