@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_head {
  this: np:hasAssertion dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion;
    np:hasProvenance dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance;
    np:hasPublicationInfo dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion a np:Assertion .
  
  dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance a np:Provenance .
  
  dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion {
  miriam-gene:860 a ncit:C16612 .
  
  lld:C0085669 a ncit:C7057 .
  
  dgn-gda:DGNbb33f90fb4e0098d0a8a2b16a45bbcdd sio:SIO_000628 miriam-gene:860, lld:C0085669;
    a sio:SIO_001121 .
}

dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_provenance {
  dgn-np:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_assertion dcterms:description
      "[Mutations in the genes encoding the interacting proteins AML1 and CBFbeta are the most common genetic abnormalities in acute leukaemia, and congenital mutations in the related AML3 gene are associated with disorders of osteogenesis.]. 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:10856244;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP284668.RAPq-tY1rkH5mAzLGb3qA9jg4bM0VEzUEfFZgLzUBg4Ls130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:22+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}