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- source_evidence_literature type ECO_0000212 NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_assertion description "[SNPs at 11 of the 16 loci (UMOD, PRKAG2, ANXA9, DAB2, SHROOM3, DACH1, STC1, SLC34A1, ALMS1/NAT8, UBE2Q2, and GCKR) were associated with incident CKD; p-values ranged from p?=?4.1e-9 in UMOD to p?=?0.03 in GCKR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_assertion evidence source_evidence_literature NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_assertion SIO_000772 21980298 NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_assertion wasDerivedFrom befree-20150227 NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_assertion wasGeneratedBy ECO_0000203 NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420995.RACSWGuDbG6ND37oyMQpeyADpg5HW4ic_l2iJ3wxHbtwg130_provenance.