Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_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." NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_assertion evidence source_evidence_literature NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_assertion SIO_000772 21920315 NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_assertion wasDerivedFrom befree-2016 NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_assertion wasGeneratedBy ECO_0000203 NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP924074.RA5B-8VGlbbCCKoNcVdqW1E6CGpIaF-bPIIWbhqn5b5tQ130_provenance.