@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE> .
@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:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_head {
  this: np:hasAssertion dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_assertion;
    np:hasProvenance dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_provenance;
    np:hasPublicationInfo dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_assertion a np:Assertion .
  
  dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_provenance a np:Provenance .
  
  dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C1623038 a ncit:C7057 .
  
  dgn-gda:DGN995230a53caef67ccfcd46da24ae4fc1 sio:SIO_000628 miriam-gene:1029, lld:C1623038;
    a sio:SIO_001121 .
}

dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_provenance {
  dgn-np:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_assertion dcterms:description
      "[In conclusion, our results demonstrate that RASSF1A and p16(INK4a) inactivation by methylation are frequent events in hepatocellular carcinoma, but not in HCA, which is in contrast to HCC without cirrhosis, viral hepatitis, storage diseases, or genetic background.]. 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:12660822;
    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:NP521050.RAPE_Gd83N44cKQEdmvDYtsQ2el7NoABOLOl05UZ96QsE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:10+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" .
}