@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_head {
  this: np:hasAssertion dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_assertion;
    np:hasProvenance dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_provenance;
    np:hasPublicationInfo dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_assertion a np:Assertion .
  
  dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_provenance a np:Provenance .
  
  dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_assertion {
  miriam-gene:6927 a ncit:C16612 .
  
  lld:C0206669 a ncit:C7057 .
  
  dgn-gda:DGNcfd86c8335dcc2f3017b2edd237ba177 sio:SIO_000628 miriam-gene:6927, lld:C0206669;
    a sio:SIO_001121 .
}

dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_provenance {
  dgn-np:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_assertion dcterms:description
      "[Biallelic inactivating mutations of HNF1A have been frequently identified in hepatocellular adenomas (HCA), rare benign liver tumors usually developed in women under oral contraceptives, and in rare cases of hepatocellular carcinomas developed in non-cirrhotic liver.]. 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:21975049;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP928752.RAmKvLU1wppO-EoByEOIAMTmIkoV1nUkSBBCZBifY2oOY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:46+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}