Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_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." NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_assertion evidence source_evidence_literature NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_assertion SIO_000772 21980298 NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_assertion wasDerivedFrom befree-20140225 NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_assertion wasGeneratedBy ECO_0000203 NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP892482.RAhPoFMhMSo0G_7MuNjUrFzZ5RxvVUJoLPv9suWTYLAIM130_provenance.