@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU> .
@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 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:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_head {
  this: np:hasAssertion dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion;
    np:hasProvenance dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_provenance;
    np:hasPublicationInfo dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion a np:Assertion .
  
  dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_provenance a np:Provenance .
  
  dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion {
  miriam-gene:80352 a ncit:C16612 .
  
  lld:C0019693 a ncit:C7057 .
  
  dgn-gda:DGN8ae3092ec1f184a3a4e68071430244de sio:SIO_000628 miriam-gene:80352, lld:C0019693;
    a sio:SIO_001122 .
}

dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_provenance {
  dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion dct: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:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}