@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I> .
@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:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_head {
  this: np:hasAssertion dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_assertion;
    np:hasProvenance dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_provenance;
    np:hasPublicationInfo dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_assertion a np:Assertion .
  
  dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_provenance a np:Provenance .
  
  dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_assertion {
  miriam-gene:5111 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN0e2184c75618e6661b17db9e6ec35019 sio:SIO_000628 miriam-gene:5111, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_provenance {
  dgn-np:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_assertion dcterms:description
      "[IgH translocations or a hyperdiploid state are emerging as early genetic signatures of MM which lead to deregulated expression of cyclin D. At present however, the major challenge remains the definition of the potential role of cytogenetic techniques and molecular profiling technologies in individual patient management.]. 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:16820292;
    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:NP420031.RAli3CQWfZBFcFFdld0r774Npa_ID6FiIneF-4FDoQD8I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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" .
}