@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0> .
@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:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_head {
  this: np:hasAssertion dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion;
    np:hasProvenance dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_provenance;
    np:hasPublicationInfo dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion a np:Assertion .
  
  dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_provenance a np:Provenance .
  
  dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion {
  miriam-gene:920 a ncit:C16612 .
  
  lld:C0007682 a ncit:C7057 .
  
  dgn-gda:DGNdf3ff2738318a6b309ecb3b752e931d4 sio:SIO_000628 miriam-gene:920, lld:C0007682;
    a sio:SIO_001121 .
}

dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_provenance {
  dgn-np:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_assertion dcterms:description
      "[These results predict the presence of HIV-1 variants with increased CCR5 affinity and reduced dependence on CCR5 and CD4 in the brains of some AIDS patients with central nervous system disease and suggest that R5 variants with increased CCR5 affinity may represent a pathogenic viral phenotype contributing to the neurodegenerative manifestations of AIDS.]. 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:12021361;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP787718.RAZTTHGoPXG5HRvIWeQqFeH4aFFWijsCveoaDPZNb85S0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}