@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw> .
@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:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_head {
  this: np:hasAssertion dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_assertion;
    np:hasProvenance dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_provenance;
    np:hasPublicationInfo dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_assertion a np:Assertion .
  
  dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_provenance a np:Provenance .
  
  dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_assertion {
  miriam-gene:100048912 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN442fb9036971a7412a2e8cf3829c39c2 sio:SIO_000628 miriam-gene:100048912,
      lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_provenance {
  dgn-np:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_assertion dcterms:description
      "[Our thorough genomic characterization of 9p21.3 suggests common variants likely account for observed disease associations and provides further support for the hypothesis that complex regulatory variation affecting ANRIL and CDKN2B gene expression may contribute to increased risk for clinically apparent and subclinical coronary artery disease and aortic disease.]. 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:23315372;
    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:NP1043314.RAJ0aT-XFYi1K7hWlQPtABMZCoR0DkoR01_P0YU6raplw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:39+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" .
}