@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_head {
  this: np:hasAssertion dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_assertion ;
    np:hasProvenance dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_provenance ;
    np:hasPublicationInfo dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_provenance a np:Provenance .
  dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_assertion {
  miriam-gene:5054 a ncit:C16612 .
  lld:C3272363 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_provenance {
  dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_assertion dcterms:description "[Among the gene polymorphisms tested in the study, association of gene polymorphisms with increasing risk of ischemic stroke was confirmed in 6 polymorphisms including angiotensin-converting enzyme insertion/deletion (ACE I/D; OR = 1.87, 95% CI = 1.45-2.42), methylenetetrahydrofolate reductase (MTHFR) C677T (OR = 1.55, 95% CI = 1.26-1.90), plasminogen activator inhibitor 1 (PAI-1) 4G/5G (OR = 1.79, 95% CI = 1.20-2.67), beta-fibrinogen (beta-Fg) -455A/G (OR = 1.48, 95% CI = 1.14-1.92), beta-Fg -148T/C (OR = 1.72, 95% CI = 1.42-2.07), apolipoprotein E (ApoE) epsilon2-4 (OR = 2.39, 95% CI = 1.94-2.95).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP532511.RAECREuy-g-zHmlGSuz2rEzyHbxPNDUatP5yx2A2i2mqs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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}