@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM> .
@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:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_head {
   this: np:hasAssertion dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_assertion ;
    np:hasProvenance dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_provenance ;
    np:hasPublicationInfo dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_assertion {
   miriam-gene:1788 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_provenance {
   dgn-np:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_assertion dcterms:description "[To evaluate the prognostic value of genetic mutations for acute myeloid leukemia (AML) patients, we examined the gene status for both fusion products such as AML1 (CBFα)-ETO, CBFβ-MYH11, PML-RARα, and MLL rearrangement as a result of chromosomal translocations and mutations in genes including FLT3, C-KIT, N-RAS, NPM1, CEBPA, WT1, ASXL1, DNMT3A, MLL, IDH1, IDH2, and TET2 in 1185 AML patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP181246.RAY2CXJAK6eSsuXf-6shp19JBitIEYGpVdcIstkwizseM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:38+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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