@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA> .
@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:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_head {
  this: np:hasAssertion dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_assertion;
    np:hasProvenance dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_provenance;
    np:hasPublicationInfo dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_assertion a np:Assertion .
  
  dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_provenance a np:Provenance .
  
  dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_assertion {
  miriam-gene:4864 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN44b47f1c6de90a3ed6c4446dc84b122a sio:SIO_000628 miriam-gene:4864, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_provenance {
  dgn-np:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_assertion dcterms:description
      "[Using gene expression and clinical data from 877 patients ranging from normal plasma cells (NPC) to relapsed MM (RMM), we applied gene expression signatures reflecting deregulation of oncogenic pathways and tumor microenvironment to highlight molecular changes that occur as NPCs transition to MM, create a high-risk MGUS gene signature, and subgroup International Staging System (ISS) stages into more prognostically accurate clusters of 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:19636021;
    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:NP900944.RA2sGQezsoc8peAFY4IVTf43dKdT0KKDdfpw9obx_qHpA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:13+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" .
}