Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion> ?p ?o ?g. }
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- NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion type Assertion NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_head.
- NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion wasGeneratedBy ECO_0000203 NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_provenance.
- NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion wasDerivedFrom lhgdn-20090331 NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_provenance.
- NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion SIO_000772 16550584 NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_provenance.
- NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_assertion evidence source_evidence_literature NP216310.RAlhNQ5MyCWk5UfZvBhMHskAPNBcHSeUsgGG3HuwwBSaY130_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.