@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ> .
@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:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_head {
  this: np:hasAssertion dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion;
    np:hasProvenance dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_provenance;
    np:hasPublicationInfo dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion a np:Assertion .
  
  dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_provenance a np:Provenance .
  
  dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion {
  miriam-gene:920 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGN6357bb923447a7d739d4c33699e6ddae sio:SIO_000628 miriam-gene:920, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_provenance {
  dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion dcterms:description
      "[Upon comparing the clinical and haematological disease characteristics of hyperdiploid versus diploid cases, the former group was characterized by a lower age, reduced incidence of anaemia, lower beta 2M levels, higher proliferative activity within the residual normal haemopoietic cells, increased expression of CD56 antigen in PC, and higher proportion of PB CD4+ T cells.]. 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:7786771;
    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:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}