Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_assertion description "[To verify the accuracy of proposed genetic modifiers influencing stroke risk in SCA, we performed genotyping for 38 published single nucleotide polymorphisms (SNPs), as well as ?-thalassemia, G6PD A(-) variant deficiency, and ?-globin haplotype in 2 cohorts of children with well-defined stroke phenotypes (130 stroke, 103 nonstroke).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_assertion evidence source_evidence_literature NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_assertion SIO_000772 21515823 NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_assertion wasDerivedFrom befree-20140225 NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_assertion wasGeneratedBy ECO_0000203 NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP714933.RALjiSlSRMET5JD-_72EwqPN_GGhQxIz_Yzsc7trN16Z0130_provenance.