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- source_evidence_literature type ECO_0000212 NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_assertion description "[Markers rs4151659 (mapping to CFB) and rs7762619 (mapping 5' of LTA) were the most strongly associated with T1D on DR3 (P=1.2 x 10(-9) and P=2 x 10(-12), respectively) and DR4 (P=4 x 10(-15) and P=8 x 10(-8), respectively) haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_assertion evidence source_evidence_literature NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_assertion SIO_000772 20054343 NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_assertion wasDerivedFrom befree-20140225 NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_assertion wasGeneratedBy ECO_0000203 NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP693864.RA3oPdvwh4HulqtwJPeB_UQiC5BaUkmBOtmDPG0pbfEPs130_provenance.