@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk> .
@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:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_head {
  this: np:hasAssertion dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_assertion;
    np:hasProvenance dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_provenance;
    np:hasPublicationInfo dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_assertion a np:Assertion .
  
  dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_provenance a np:Provenance .
  
  dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_assertion {
  miriam-gene:283120 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN9c72e99f97f9fa223950c8811af96cef sio:SIO_000628 miriam-gene:283120, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_provenance {
  dgn-np:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_assertion dcterms:description
      "[Progression from adrenal adenoma to carcinoma involves a monoclonal proliferation of cells which, among other defects, have undergone chromosomal duplication at the 11p15.5 locus leading to overexpression of the IGF2 gene and abrogation of expression of the CDKN1C and H19 genes.]. 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:12956790;
    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:NP738659.RAEz9I2FHi0u4XRJgseQ76U_FdzEfRT9XsimWGFY7pnDk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:28+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" .
}