Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion description "[The Cx26 mutant W77R, which has been implicated in autosomal recessive deafness, also failed to form functional gap channels by itself but did not significantly interfere with the function of wildtype Cx26.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion evidence source_evidence_literature NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion SIO_000772 9856479 NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion wasDerivedFrom befree-2016 NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion wasGeneratedBy ECO_0000203 NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_provenance.