Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_assertion description "[Polymorphic variation in ALDH2, XPD and MGMT genes may be of importance for ESCC susceptibility. Polymorphic variation in CYP2A6 and MGMT are associated with ESCC metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_assertion evidence source_evidence_literature NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_assertion SIO_000772 20128036 NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_assertion wasDerivedFrom gad-20150221 NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_assertion wasGeneratedBy ECO_0000203 NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP163611.RA3PId_WC3V5dQsocl-8rIhdKfRA0maDcM-n_vYomAVpk130_provenance.