@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M> .
@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/v4.0.0/void/> .
dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_head {
  this: np:hasAssertion dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_assertion ;
    np:hasProvenance dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_provenance ;
    np:hasPublicationInfo dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_assertion a np:Assertion .
  dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_provenance a np:Provenance .
  dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_assertion {
  miriam-gene:10148 a ncit:C16612 .
  lld:C0023449 a ncit:C7057 .
  dgn-gda:DGN8ca47b86737e8472d409a3bbbd56eead sio:SIO_000628 miriam-gene:10148 , lld:C0023449 ;
    a sio:SIO_001121 .
}
dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_provenance {
  dgn-np:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_assertion dcterms:description "[High-resolution genomic profiling of genetic alterations and gene expression has revolutionized our understanding of the genetic basis of ALL, and has identified several alterations associated with poor outcome, including mutations of the lymphoid transcription factor gene IKZF1 (IKAROS), activating mutations of Janus kinases, and rearrangement of the lymphoid cytokine receptor gene CRLF2.]. 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:21370430 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP876834.RAmGFeVDhAxFXx3jPpeV4HFn3Li65awlSAtpGzLg3Ft9M130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:22+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}