Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_assertion description "[The present study demonstrated no evidence of association between individual SELP or PSGL-1 SNPs or haplotypes with incident CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_assertion evidence source_evidence_literature NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_assertion SIO_000772 20376705 NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_assertion wasDerivedFrom befree-20140225 NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_assertion wasGeneratedBy ECO_0000203 NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208219.RACzeJ5wrVb-r08447ylqu2l1DtmbbukzQGNFYF_QyWq8130_provenance.