@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo> .
@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/v4.0.0/void/> .

dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_head {
  this: np:hasAssertion dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_assertion;
    np:hasProvenance dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_provenance;
    np:hasPublicationInfo dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_assertion a np:Assertion .
  
  dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_provenance a np:Provenance .
  
  dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_assertion {
  miriam-gene:3757 a ncit:C16612 .
  
  lld:C0553580 a ncit:C7057 .
  
  dgn-gda:DGN20e1d67cb713fe2eeb7837a1902dc646 sio:SIO_000628 miriam-gene:3757, lld:C0553580;
    a sio:SIO_001121 .
}

dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_provenance {
  dgn-np:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_assertion dcterms:description
      "[Because of the high heterogeneity of EWS gene fusions with FLI1 and ERG genes due to variable chromosomal breakpoint locations in Ewing tumors (ET) (14 different chimeric transcripts identified so far), we evaluated the clinical impact of the expression of diverse fusion transcripts in ET patients.]. 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:8648380;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1351048.RARU7m7t-VjJ6J3MgnLP5odrG0Kb5IxrDHWA2_GC1RkSo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:58+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}