@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo> .
@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:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_head {
  this: np:hasAssertion dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion;
    np:hasProvenance dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_provenance;
    np:hasPublicationInfo dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion a np:Assertion .
  
  dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_provenance a np:Provenance .
  
  dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion {
  miriam-gene:6580 a ncit:C16612 .
  
  lld:C0206698 a ncit:C7057 .
  
  dgn-gda:DGNb3ae555bd73c4eabc2c773e58a70d4b9 sio:SIO_000628 miriam-gene:6580, lld:C0206698;
    a sio:SIO_001121 .
}

dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_provenance {
  dgn-np:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_assertion dcterms:description
      "[Conclusion: Development of HCC and CGC is accompanied by the appearance of aberrant OCT1 variants that, together with decreased OCT1 expression, may dramatically affect the ability of sorafenib to reach active intracellular concentrations in these tumors.]. 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:23532667;
    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:NP235212.RAZeIGvQpYikSjXijgLdoVk4gl-ClElBHkZ9juBK4Vjyo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}