Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_assertion description "[Additionally, 698 CNPs showed significant differences with false discovery rate (FDR)<0.01 among the 10 populations and these loci overlap with known disease-associated or pharmacogenetic-related genes such as CFHR3 and CFHR1 (age related macular degeneration), GSTTI (metabolism of various carcinogenic compounds and cancers) and UGT2B17 (prostate cancer and graft-versus-host disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_assertion evidence source_evidence_literature NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_assertion SIO_000772 21677662 NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_assertion wasDerivedFrom befree-20140225 NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_assertion wasGeneratedBy ECO_0000203 NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP334693.RABoiMOklFGAsVJADL-pqeZqkkbtCCaxUK87CM8-QvpKs130_provenance.