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- source_evidence_literature type ECO_0000212 NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_assertion description "[There is a significant association of CD with the single nucleotide polymorphisms (SNPs) in ATG16L1 (odds ratio [OR] 1.36 [1.15-1.60], P = 2.7 � 10(-6) for allele G), IRGM (OR 1.56 [1.21-1.93], P = 3.9 � 10(-4) for allele C), and ITLN1 (OR 1.55 [1.28-1.88], P = 4.9 � 10(-4) for allele C).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_assertion evidence source_evidence_literature NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_assertion SIO_000772 22573572 NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_assertion wasDerivedFrom befree-20140225 NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_assertion wasGeneratedBy ECO_0000203 NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP770066.RAkOMsuT7wO_1GhUJKCZU6ZhGcx6_wg_JiWNSCb35IK1g130_provenance.