@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ> .
@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/v4.0.0/void/> .

dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_head {
  this: np:hasAssertion dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_assertion;
    np:hasProvenance dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_provenance;
    np:hasPublicationInfo dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_assertion a np:Assertion .
  
  dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_provenance a np:Provenance .
  
  dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_assertion {
  miriam-gene:336 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN909b651e28cde5838a5fb26142a83193 sio:SIO_000628 miriam-gene:336, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_provenance {
  dgn-np:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_assertion dcterms:description
      "[In a case-control analysis of 484 male CAD patients and 498 male controls, individuals carrying the 'CC' genotype for the APOAII rs5082 polymorphism had significantly lower risk of CAD than the 'T' allele carriers (OR=0.57, 95% CI 0.39-0.84, p=0.004).]. 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:18179799;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP648693.RAPoO9fZM5F-BL2eaCeR9USTNSFLJWuCOW5uH-sO12YhQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:39+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:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}