Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_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." NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_assertion evidence source_evidence_literature NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_assertion SIO_000772 21920315 NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_assertion wasDerivedFrom befree-20150227 NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_assertion wasGeneratedBy ECO_0000203 NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP426608.RAVNAm6pJpvOXUSNXrD4SdnC4o5fYUqr1Vpt288Pm4GXA130_provenance.