@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE> .
@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:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_head {
  this: np:hasAssertion dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion;
    np:hasProvenance dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_provenance;
    np:hasPublicationInfo dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion a np:Assertion .
  
  dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_provenance a np:Provenance .
  
  dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion {
  miriam-gene:23541 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGNc1e8731c5b51fce5313b91503870a9ba sio:SIO_000628 miriam-gene:23541, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_provenance {
  dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion dcterms:description
      "[The higher risk that is associated with CA compared with SPF justifies routine cytogenetic studies in all patients with MM at diagnosis and whenever additional treatment decisions are considered, such as in planning HDT either for initial response consolidation, at the time of primary unresponsiveness to induction therapy, or at relapse.]. 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:12877670;
    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:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}