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- source_evidence_literature type ECO_0000212 NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_assertion description "[Statistically significant results found for the various QTs and SNPs were: rs3774933, rs230528, rs230521, rs1005819 and rs1609798 (intronic, NFKB1) with APOB; rs5361 (Missense, R greatr than S, SELE) and rs4648004 (Intronic, NFKB1) with FBG; rs4220 (Missense, K greater than R, FGB) with HCY; and rs3025035 (Intronic, VEGFA) with CHOL-H. SNPs in SELE, VEGFA, FGB and NFKB1 genes impact significantly on levels of quantitative precursors of CAD in Marwaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_assertion evidence source_evidence_literature NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_assertion SIO_000772 22116284 NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_assertion wasDerivedFrom befree-20150227 NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_assertion wasGeneratedBy ECO_0000203 NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP689763.RAbbKFEC4xL4PKOds7K706_IoPFBBExKtJe9r16UI252Y130_provenance.