@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ> .
@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:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_head {
  this: np:hasAssertion dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion;
    np:hasProvenance dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_provenance;
    np:hasPublicationInfo dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion a np:Assertion .
  
  dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_provenance a np:Provenance .
  
  dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion {
  miriam-gene:920 a ncit:C16612 .
  
  lld:C0007099 a ncit:C7057 .
  
  dgn-gda:DGN1786ce36d8746002930bfc786aa38ef2 sio:SIO_000628 miriam-gene:920, lld:C0007099;
    a sio:SIO_001121 .
}

dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_provenance {
  dgn-np:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_assertion dcterms:description
      "[After adjustment for anal cytological diagnoses at study entry, HIV status and CD4 count, and detection of HPV types other than type 16, men with HPV16 NPL variants were 3.2 times (95% confidence interval, 1.0-10.3) more likely to develop anal CIS than were those with PL variants.]. 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:9731493;
    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:NP371219.RA53e7E1EA-k_j5ojeAbae_IC1FF-PGsoG8S6RKZ9Q0AQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:37+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" .
}