Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_assertion description "[No association between XPD Lys751Gln or XRCC1 Arg399Gln polymorphisms and the presence or the severity of CAD was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_assertion evidence source_evidence_literature NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_assertion SIO_000772 18043991 NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_assertion wasDerivedFrom befree-20140225 NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_assertion wasGeneratedBy ECO_0000203 NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP277054.RAUc37TP_xWKOW764znn85MAzrE8KgkKUeverGAJ1V3q4130_provenance.