@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk> .
@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:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_head {
  this: np:hasAssertion dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_assertion;
    np:hasProvenance dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_provenance;
    np:hasPublicationInfo dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_assertion a np:Assertion .
  
  dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_provenance a np:Provenance .
  
  dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_assertion {
  miriam-gene:3107 a ncit:C16612 .
  
  lld:C0019693 a ncit:C7057 .
  
  dgn-gda:DGN7487f08649c544479ce73b9e0fe0a8d1 sio:SIO_000628 miriam-gene:3107, lld:C0019693;
    a sio:SIO_001122 .
}

dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_provenance {
  dgn-np:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_assertion dcterms:description
      "[A genome-wide association study of people with incident human immunodeficiency virus (HIV) infection selected from nine different cohorts identified allelic polymorphisms, which associated with either viral set point (HCP5 and 5' HLA-C) or with HIV disease progression (RNF39 and ZNRD1).]. 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:19693088;
    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:NP73598.RAbBW8msVtqme17bS3ifEA1Ok5ao0f1DUrDcWPY5WNDSk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+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" .
}