Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion> ?p ?o ?g. }
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- NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_assertion type Assertion NP1411093.RAEBgRNkiZEQNEbbxUFbfghVQ2ttXPBkw2ctFPZUV3-5M130_head.
- 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.