@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0> .
@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 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:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_head {
  this: np:hasAssertion dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion;
    np:hasProvenance dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_provenance;
    np:hasPublicationInfo dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion a np:Assertion .
  
  dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_provenance a np:Provenance .
  
  dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN563d59f0663cd525283f5b9c43159f85 sio:SIO_000628 miriam-gene:7248, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_provenance {
  dgn-np:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_assertion dc:description
      "[Our results suggest that there is a heterogeneous, non-systematic but almost universal presence of activated oncogenes and tumour suppressor genes in the plasma cells of patients with multiple myeloma and that disease progression is associated with the accumulation of a variety of secondary genetic changes which confer increased malignant behaviour.]. 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:7696921;
    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:NP372227.RAAobj6GLVS0NAp8rz-jn1bjXe-BsmpWJwigecOslSHV0130_publicationInfo {
  this: dc:created "2014-10-02T12:35:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}