@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A> .
@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:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_head {
  this: np:hasAssertion dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion;
    np:hasProvenance dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_provenance;
    np:hasPublicationInfo dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion a np:Assertion .
  
  dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_provenance a np:Provenance .
  
  dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion {
  miriam-gene:6319 a ncit:C16612 .
  
  lld:C0155626 a ncit:C7057 .
  
  dgn-gda:DGNf07cf03ce8e63bf498119b243fcce86e sio:SIO_000628 miriam-gene:6319, lld:C0155626;
    a sio:SIO_001121 .
}

dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_provenance {
  dgn-np:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_assertion dcterms:description
      "[In logistic regression analysis with age, body mass index, hypertension, diabetes, smoking and alcohol consumption as covariates, men with the TT genotype had an increased risk for SCD and AMI compared to CC carriers (OR=3.0, P=0.011; and OR=3.7, P=0.003).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:16793047;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  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:NP657542.RAGD09USbzQT7ZGcVRi2tZ7FFXlUYixwl5NQbM7qELa5A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:36+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}