@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic> .
@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:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_head {
  this: np:hasAssertion dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_assertion;
    np:hasProvenance dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_provenance;
    np:hasPublicationInfo dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_assertion a np:Assertion .
  
  dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_provenance a np:Provenance .
  
  dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_assertion {
  miriam-gene:4297 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGNab9fb34c2325364a1caa8034d2bc54ad sio:SIO_000628 miriam-gene:4297, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_provenance {
  dgn-np:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_assertion dcterms:description
      "[Translocations and other rearrangements of the MLL gene at chromosome band 11q23 are biologically and clinically important molecular abnormalities in infant acute leukemias, leukemias associated with chemotherapeutic topoisomerase II poisons and, less often, acute leukemias in adults or myelodysplastic syndrome.]. 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:19277575;
    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:NP501852.RAXxJCjcJzlqS55-fqbK78_Bm4Lxp3CfLUZc8CtQGoYic130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}