@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24> .
@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:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_head {
  this: np:hasAssertion dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion;
    np:hasProvenance dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_provenance;
    np:hasPublicationInfo dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion a np:Assertion .
  
  dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_provenance a np:Provenance .
  
  dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion {
  miriam-gene:6003 a ncit:C16612 .
  
  lld:C0041107 a ncit:C7057 .
  
  dgn-gda:DGN06d266bcb7fa2d2532be9f6ddcb52e80 sio:SIO_000628 miriam-gene:6003, lld:C0041107;
    a sio:SIO_001121 .
}

dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_provenance {
  dgn-np:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_assertion dcterms:description
      "[By analyzing several genes with very high (`spiked`) expression in individual cases, we identified clusters with different biologic characteristics, such as samples with MALT1 translocations having high expression of MALT1 and RARA, samples with plasmacytic differentiation having high FKBP11 expression, and samples with high RGS13 expression tending to have trisomy 3 and reactive follicles.]. 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:18974375;
    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:NP168424.RAqxJETAT2NLbGf7EA1hHy_pBtWjLGAns53Ib4YUSUD24130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}