@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c> .
@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:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_head {
  this: np:hasAssertion dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_assertion;
    np:hasProvenance dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_provenance;
    np:hasPublicationInfo dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_assertion a np:Assertion .
  
  dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_provenance a np:Provenance .
  
  dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_assertion {
  miriam-gene:4613 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGNc98c7e8a18eb430ed77fbdbc08c020b5 sio:SIO_000628 miriam-gene:4613, lld:C0035335;
    a sio:SIO_001121 .
}

dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_provenance {
  dgn-np:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_assertion dcterms:description
      "[Our results demonstrated that some copy number changes thought to belong to early (MDM4 gain) or late stage (MYCN and E2F3 gain) of retinoblastoma are already present in retinoma at the same (for MDM4) or at lower (for MYCN and E2F3) copy number variation respect to retinoblastoma.]. 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:18785023;
    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:NP582542.RANiGYnEu_T13JdqCxr9s7sI7HZEn57tFNakbGYOk-D3c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:28+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: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" .
}