Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_assertion description "[Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_assertion evidence source_evidence_literature NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_assertion SIO_000772 11090341 NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_assertion wasDerivedFrom befree-20140225 NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_assertion wasGeneratedBy ECO_0000203 NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP242863.RAzCuqLu7HoSJ6-IWRlYZ2aDKO2qjyxIrhYGzteONxATk130_provenance.