@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do> .
@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:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_head {
  this: np:hasAssertion dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_assertion;
    np:hasProvenance dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_provenance;
    np:hasPublicationInfo dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_assertion a np:Assertion .
  
  dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_provenance a np:Provenance .
  
  dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_assertion {
  miriam-gene:3207 a ncit:C16612 .
  
  lld:C0333875 a ncit:C7057 .
  
  dgn-gda:DGNe43eaae4e60ab1d69e2269ecd1195a6b sio:SIO_000628 miriam-gene:3207, lld:C0333875;
    a sio:SIO_001121 .
}

dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_provenance {
  dgn-np:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_assertion dcterms:description
      "[Area under the receiver operating characteristic (ROC) curve (AUC) demonstrated that methylation of SOX1, HOXA11 and CADM1 could discriminate between HSIL cases and controls with high sensitivity and specificity (AUC 0.910, 0.844 and 0.760, respectively).]. 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:19609949;
    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:NP913935.RA9T-iQDkFzbqBQkz5F15jVlQZBrpu1dYeJjFMWioa0Do130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:21+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" .
}