Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion> ?p ?o ?g. }
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- NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion type Assertion NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_head.
- NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion description "[Recessive mutant alleles of MYO7A, USH1C, CDH23, and PCDH15 cause non-syndromic deafness or type 1 Usher syndrome (USH1) characterised by deafness, vestibular areflexia, and vision loss due to retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion evidence source_evidence_literature NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion SIO_000772 21940737 NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion wasDerivedFrom befree-20150227 NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_assertion wasGeneratedBy ECO_0000203 NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.