@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU> .
@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:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_head {
  this: np:hasAssertion dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_assertion;
    np:hasProvenance dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_provenance;
    np:hasPublicationInfo dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_assertion a np:Assertion .
  
  dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_provenance a np:Provenance .
  
  dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_assertion {
  miriam-gene:412 a ncit:C16612 .
  
  lld:C0206708 a ncit:C7057 .
  
  dgn-gda:DGN7290ed5c1220406a7ec75d5134226708 sio:SIO_000628 miriam-gene:412, lld:C0206708;
    a sio:SIO_001121 .
}

dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_provenance {
  dgn-np:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_assertion dcterms:description
      "[To evaluate whether human papillomavirus (HPV) genotyping for the selected oncogenic HPV types can improve the efficacy of HPV DNA testing in predicting cervical intraepithelial neoplasia (CIN 2/3) in women with mildly abnormal Pap results, we compared HPV DNA testing and HPV genotyping for eight oncogenic types (16, 18, 31, 33, 35, 45, 52 and 58) in Pap specimens with abnormal results (HSIL, 20 cases; LSIL, 42 cases; ASC-US, 94 cases) and follow-up biopsies.]. 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:18500260;
    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:NP242184.RAliS6Oic0vgdyOc3CdcizHVeL7LovkA011l_R5764hlU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:15+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" .
}