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<http://rdf.disgenet.org/nanopublications.trig#NP589139.RAacT9rf8eMcSiggV9abPmlUOATUVS6MlgAFiG-B-8pCI130_assertion> <http://purl.org/dc/terms/description> "[Examination of 9 single nucleotide polymorphisms (SNPs) in this group revealed that homozygotes for APOA4 S347 had significantly increased risk of CHD [hazard ratio (HR) of 2.07 (95%CI 1.04 to 4.12)], whereas men homozygous for APOC3 1100T were protected [HR 0.28 (95%CI 0.09 to 0.87)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP589139.RAacT9rf8eMcSiggV9abPmlUOATUVS6MlgAFiG-B-8pCI130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://purl.org/pav/2.0/importedOn> "2014-02-25"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP589139.RAacT9rf8eMcSiggV9abPmlUOATUVS6MlgAFiG-B-8pCI130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP589139.RAacT9rf8eMcSiggV9abPmlUOATUVS6MlgAFiG-B-8pCI130_provenance> .
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