Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_assertion description "[There were no significant differences in the genotype, allele and haplotype frequencies of P-selectin gene polymorphisms between the group of patients with ischemic stroke and the control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_assertion evidence source_evidence_literature NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_assertion SIO_000772 18034324 NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_assertion wasDerivedFrom befree-20140225 NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_assertion wasGeneratedBy ECO_0000203 NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP484146.RAu_wQXprjvpfG23nlUlur-O99GtU5IXH2_YfhklTYNSs130_provenance.