@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk> .
@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:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_head {
  this: np:hasAssertion dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_assertion;
    np:hasProvenance dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_provenance;
    np:hasPublicationInfo dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_assertion a np:Assertion .
  
  dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_provenance a np:Provenance .
  
  dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_assertion {
  miriam-gene:5327 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGN3eb761062c9488809f7a1cfbb9b76d17 sio:SIO_000628 miriam-gene:5327, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_provenance {
  dgn-np:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_assertion dcterms:description
      "[Both approaches (association analysis and gametic disequilibrium) revealed the same gene combinations contributing to the CAD risk factors. NOS3 and APOA1 markers were in gametic disequilibrium in the patients and both of them were associated with LDL. F13 and AGT were associated with systolic and diastolic blood pressure and two-locus gametic disequilibrium between F13 and AGT polymorphisms observed in the patients.]. 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:11507973;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP53095.RAl-Xi87IPOGrmHRbSCOaPGEBtIv_7Fx6XzCL_ohAuySk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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>,
      <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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}