@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA> .
@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:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_head {
  this: np:hasAssertion dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_assertion;
    np:hasProvenance dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_provenance;
    np:hasPublicationInfo dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_assertion a np:Assertion .
  
  dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_provenance a np:Provenance .
  
  dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_assertion {
  miriam-gene:2078 a ncit:C16612 .
  
  lld:C0023449 a ncit:C7057 .
  
  dgn-gda:DGNa7ceed269a313aa1c6b6caf3036f2570 sio:SIO_000628 miriam-gene:2078, lld:C0023449;
    a sio:SIO_001121 .
}

dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_provenance {
  dgn-np:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_assertion dcterms:description
      "[This identified 52 somatic non-synonymous mutations in 32 genes, many of which were novel, including the transcriptional coactivators CREBBP and NCOR1, the transcription factors ERG, SPI1, TCF4 and TCF7L2, components of the Ras signalling pathway, histone genes, genes involved in histone modification (CREBBP and CTCF), and genes previously shown to be targets of recurring DNA copy number alteration in ALL.]. 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:21390130;
    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:NP464841.RAa3VgPxi6ZId5wSVSzJPwtpJMsnR81wwUC7xywlS_OAA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:39+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" .
}