Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_assertion wasGeneratedBy ECO_0000203 NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_assertion wasDerivedFrom gad-20150221 NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_assertion SIO_000772 17687452 NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_assertion evidence source_evidence_literature NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.
- NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_assertion description "[Our findings indicate a reduced NMSC risk in relation to XPD Asp312Asn and Lys751Gln variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109963.RACg2hHwVe3PQcT6f8sQiLJS59I1WCPaKb_VVO-G9KQOA130_provenance.