Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP941457.RAY_-koa_i7JQr2JrMgtHurW15TOVntdmSw9UNfW0INVs130_provenance.