Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_assertion description "[Our study shows that variants in these three loci confer consistent disease risks in patients of European descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_assertion evidence source_evidence_literature NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_assertion SIO_000772 19279021 NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_assertion wasDerivedFrom gad-20130706 NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_assertion wasGeneratedBy ECO_0000203 NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP69932.RAstD3iHSU4x59REerDiHfR5P7X2TZNgpYOMrwGKfbaLg130_provenance.