@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4> .
@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/v3.0.0/void/> .

dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_head {
  this: np:hasAssertion dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_assertion;
    np:hasProvenance dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_provenance;
    np:hasPublicationInfo dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_assertion a np:Assertion .
  
  dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_provenance a np:Provenance .
  
  dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGNe48f9b7be2adcf1e1ecaf8c650fc895a sio:SIO_000628 miriam-gene:3342, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_provenance {
  dgn-np:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_assertion dcterms:description
      "[Our CGH results suggest that the gain of 20q and deletion of 8p are late genetic alterations in HCC, because the incidence of these alterations was obviously increased in the advanced clinical stages.]. 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:10959090;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP470748.RAFtRj81N3d9lcw7ndabSLmkkTpbKAaGkphxnLKioRKF4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:17+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}