@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw> .
@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:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_head {
  this: np:hasAssertion dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_assertion;
    np:hasProvenance dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_provenance;
    np:hasPublicationInfo dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_assertion a np:Assertion .
  
  dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_provenance a np:Provenance .
  
  dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_assertion {
  miriam-gene:4297 a ncit:C16612 .
  
  lld:C0220621 a ncit:C7057 .
  
  dgn-gda:DGNd77edd24779ccf43b2dd81ba92b5537e sio:SIO_000628 miriam-gene:4297, lld:C0220621;
    a sio:SIO_001121 .
}

dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_provenance {
  dgn-np:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_assertion dcterms:description
      "[The distribution of MLL breakpoints for clinical subtypes (acute lymphoblastic leukemia, acute myeloid leukemia, pediatric and adult) and fused translocation partner genes (TPGs) will be presented, including novel MLL fusion genes.]. 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:19262598;
    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:NP608199.RAnAsRxD1xbcyiyM8X9Z2OPUmLtSqxXGKc1DbkrLzdeaw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:05+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" .
}