@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk> .
@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:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_head {
  this: np:hasAssertion dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion;
    np:hasProvenance dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance;
    np:hasPublicationInfo dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion a np:Assertion .
  
  dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance a np:Provenance .
  
  dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion {
  miriam-gene:10 a ncit:C16612 .
  
  lld:C0302592 a ncit:C7057 .
  
  dgn-gda:DGN912de7dd7ea97320c3f90cd564d3f76b sio:SIO_000628 miriam-gene:10, lld:C0302592;
    a sio:SIO_001122 .
}

dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance {
  dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion dcterms:description
      "[The results reported in this study suggest that NAT2 polymorphism is a genetic susceptibility factor involved in the carcinogenesis of cervical cancer, and also that the analysis of the allelic profile of populations in different geographic locations may help to understand the incidence of cervical cancer worldwide.]. 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:12474054;
    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:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}