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<http://linkedlifedata.com/resource/umls/id/C0027051> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN050597a3f6102c17916e63db43000e0a> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/9619> <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN050597a3f6102c17916e63db43000e0a> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0027051> <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN050597a3f6102c17916e63db43000e0a> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_assertion> <http://purl.org/dc/terms/description> "[The human ABCG1 -367G>A polymorphism (rs57137919) showed a significantly decreased risk for CAD and myocardial infarction (MI) in a dominant model (adjusted OR = 0.73, p = 0.033 for CAD, and adjusted OR = 0.65, p = 0.014 for MI, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_assertion> <http://purl.org/ontology/wi/core#evidence> <http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_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#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000212> <http://rdf.disgenet.org/nanopublications.trig#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_provenance> .
<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#NP765955.RAnHrKotLhBcCbLWOOjV2xdGQPQsUZmPERiCYVArHW41k130_provenance> .
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