Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_assertion description "[In white individuals, the A1166C 3'-UTR variant of angiotensin II type 1 receptor (AT1R) has been associated with CKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_assertion evidence source_evidence_literature NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_assertion SIO_000772 16396964 NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_assertion wasDerivedFrom befree-20140225 NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_assertion wasGeneratedBy ECO_0000203 NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217178.RAWwEVmGt3EPS-7pFQeFbNdtPeeQtLiXYOrblPs-V9vtw130_provenance.