Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion> ?p ?o ?g. }
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- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion type Assertion NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_head.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion wasGeneratedBy ECO_0000203 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion wasDerivedFrom befree-2016 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion SIO_000772 16550584 NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion evidence source_evidence_literature NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.
- NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_assertion description "[Missense mutations in CDH23 have been associated with presbycusis and DFNB12, whereas null alleles cause the majority of Usher 1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541240.RAyF3wairV1clvygwCjpSq-6fo1P0Kfgsy_OMsmPZOGJY130_provenance.