@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_head {
  this: np:hasAssertion dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_assertion;
    np:hasProvenance dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_provenance;
    np:hasPublicationInfo dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_publicationInfo;
    a np:Nanopublication .
  
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dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_assertion {
  miriam-gene:3569 a ncit:C16612 .
  
  lld:C0020443 a ncit:C7057 .
  
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dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_provenance {
  dgn-np:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_assertion dcterms:description
      "[Multivariable logistic regression analysis and a stepwise forward selection procedure revealed that 11 different polymorphisms were significantly (P &lt; 0.005) associated with ACI in women or men or in individuals with or without hyper-tension, hypercholesterolemia, or diabetes mellitus: the 584C--&gt;T polymorphism of LIPG, 5665G--&gt;T of EDN1, and G--&gt;A of CCL11 in women; 677C--&gt;T of MTHFR, 1323C--&gt;T of ITGB2, 3932T--&gt;C of APOE, and -231A--&gt;G of EDNRA in men; -572 G --&gt;C of IL6 in hypertensive individuals; -403G--&gt;A of CCL5 and G--&gt;A of COMT in individuals with hypercholesterolemia; and 3932T--&gt; C of APOE and A--&gt;G of TNFSF4 in diabetic individuals.]. 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:NP497340.RALMIR9-FUhfrVQ_Y8JHeZ7elfsEqiX97WuE9N87MrCe4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:33+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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