@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M> .
@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:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_head {
  this: np:hasAssertion dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion;
    np:hasProvenance dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_provenance;
    np:hasPublicationInfo dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion a np:Assertion .
  
  dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_provenance a np:Provenance .
  
  dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion {
  miriam-gene:4928 a ncit:C16612 .
  
  lld:C0220621 a ncit:C7057 .
  
  dgn-gda:DGNa00a4405ff9f40cddf551f2687053e6c sio:SIO_000628 miriam-gene:4928, lld:C0220621;
    a sio:SIO_001121 .
}

dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_provenance {
  dgn-np:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_assertion dcterms:description
      "[The aim of this study was to determine the incidence of rearrangements of NUP98 (the gene coding for nucleoporin 98kDa protein) in childhood acute myeloid leukemia (AML) and selected patients with 11p13-15 rearrangements.]. 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:15951287;
    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:NP824893.RAaHGsZlUWKqAJYEBdoh5vtfLvBg6-NOihR2QRWyIdI5M130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
}