Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_assertion description "[We compared cadherin 23 (Cdh23) mRNA and protein variants in the inner ear and retina of wild-type and mutant mice and primates to better understand the pleiotropic effects of Cdh23 mutations, and specifically to understand the absence of retinal degeneration in Cdh23 mutant mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_assertion evidence source_evidence_literature NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_assertion SIO_000772 19756182 NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_assertion wasDerivedFrom befree-2016 NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_assertion wasGeneratedBy ECO_0000203 NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP763405.RAADHiU5pBeK2pPw7wOg3HO9ipFtpU3_VG8IN6ol02jVQ130_provenance.