Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_assertion description "[Ten non-synonymous single nucleotide polymorphisms (nsSNPs), which were recently associated with colorectal cancer risk in a comprehensive, array based study (AKAP9 M463I, DKK3 G335R, AMPD1 Q12X, LIPC L356F, PSMB9 V32I, THBS1 N700S, CA6 S90G, ASCC3 C1995S, DHX36 S416C and CPA4 G303C) were re-evaluated in the present study based on 626 German familial non-HNPCC colorectal cancer patients and 736 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_assertion evidence source_evidence_literature NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_assertion SIO_000772 18619730 NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_assertion wasDerivedFrom befree-20150227 NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_assertion wasGeneratedBy ECO_0000203 NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP886147.RA4n2U_GsLC5rPVvNvaS6320tT1m7waJxoSt8eZtTKAtI130_provenance.