@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU> .
@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:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_head {
  this: np:hasAssertion dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_assertion;
    np:hasProvenance dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_provenance;
    np:hasPublicationInfo dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_assertion a np:Assertion .
  
  dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_provenance a np:Provenance .
  
  dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_assertion {
  miriam-gene:5054 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGNf32920e1d82f58e0be71251a6b8d074a sio:SIO_000628 miriam-gene:5054, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_provenance {
  dgn-np:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_assertion dcterms:description
      "[In a sample of both 83 healthy individuals and 105 young patients with coronary artery disease from Sweden, the frequency of the 4G allele is roughly 0.5, and those individuals homozygous for the 4G allele have higher levels of PAI-1 than those with other genotypes (29% higher).]. 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:1456879;
    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:NP417531.RAxX9yigSTdFNdD89IcMhPCkrHDGXswEUtTXUrzeXpsWU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:54+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" .
}