@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw> .
@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:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_head {
  this: np:hasAssertion dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_assertion;
    np:hasProvenance dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_provenance;
    np:hasPublicationInfo dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_assertion a np:Assertion .
  
  dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_provenance a np:Provenance .
  
  dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_assertion {
  miriam-gene:6667 a ncit:C16612 .
  
  lld:C0007847 a ncit:C7057 .
  
  dgn-gda:DGN2da76b890aafd73a9193e356c181841e sio:SIO_000628 miriam-gene:6667, lld:C0007847;
    a sio:SIO_001121 .
}

dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_provenance {
  dgn-np:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_assertion dcterms:description
      "[Comparison of the two groups revealed that isolates from cervical cancers predominantly carry changes in sequences of YY1 binding sites (especially at nucleotide 7519), while variants from asymptomatic carriers contained nucleotide changes within or close to transcription binding sites for AP-1, Oct-1, NF1, Tef-1, Tef-2, Sp1, YY1 and viral E2.]. 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:11595585;
    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:NP705145.RAopMcH06pioNxkOTwdJvf10W9yF2p5aRBZywUeeqO5yw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}