@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM> .
@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:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_head {
  this: np:hasAssertion dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_assertion;
    np:hasProvenance dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_provenance;
    np:hasPublicationInfo dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_assertion a np:Assertion .
  
  dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_provenance a np:Provenance .
  
  dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_assertion {
  miriam-gene:6928 a ncit:C16612 .
  
  lld:C0677886 a ncit:C7057 .
  
  dgn-gda:DGN4e00f36f81081d02673c62560848eade sio:SIO_000628 miriam-gene:6928, lld:C0677886;
    a sio:SIO_001121 .
}

dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_provenance {
  dgn-np:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_assertion dcterms:description
      "[HNF1B is overexpressed in clear cell epithelial ovarian cancer, and we observed epigenetic silencing in serous epithelial ovarian cancer, leading us to hypothesize that variation in this gene differentially associates with epithelial ovarian cancer risk according to histological subtype.]. 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:23535649;
    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:NP883787.RASna-LW2YxSZgM_Imeclj4mSnARCXDWnz4caxvg6VtvM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}