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- source_evidence_literature type ECO_0000212 NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_assertion description "[Single-SNP analysis demonstrated significant associations of the CARD15_R702W variation and the NALP12_In9 T-allele with AD (P = 0.008 and P = 0.03, resp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_assertion evidence source_evidence_literature NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_assertion SIO_000772 17620097 NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_assertion wasDerivedFrom befree-2016 NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_assertion wasGeneratedBy ECO_0000203 NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP619207.RAqahZuYQix5-Wcrk3v0r1zjyz-KudoLB5hww9u4ve4JQ130_provenance.