Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_assertion description "[We also show that�a mutation of human Connexin 31, which causes erythrokeratoderma variabilis, induces ER stress and p63-dependent epidermal apoptosis in the zebrafish embryo, thus implicating this pathway in the pathogenesis of inherited disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_assertion evidence source_evidence_literature NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_assertion SIO_000772 21920315 NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_assertion wasDerivedFrom befree-20140225 NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_assertion wasGeneratedBy ECO_0000203 NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP481310.RAkdKnN3WBnL86Hy8wgpW4XbUfPEbJF5PzGC1hV4xfK5M130_provenance.