Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_assertion description "[The risk in the carriers of the ERCC2 751Gln variant was increased by a positive cancer history in first degree relatives (OR 4.97; 95 % CI 1.98-12.48).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_assertion evidence source_evidence_literature NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_assertion SIO_000772 22544315 NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_assertion wasDerivedFrom befree-20150227 NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_assertion wasGeneratedBy ECO_0000203 NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382193.RA-Lrxw-l1flUnHhkmpxLlJPjlxxcpIhPNC7qpH99M7fo130_provenance.