Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_assertion evidence source_evidence_literature NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_assertion SIO_000772 19426954 NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_assertion wasDerivedFrom befree-20140225 NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_assertion wasGeneratedBy ECO_0000203 NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP920620.RAhnkQt-H4112zTRZeh0njmn8Rvc5sjq0QwXXCZGN-OPE130_provenance.