@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4> .
@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:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_head {
  this: np:hasAssertion dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_assertion ;
    np:hasProvenance dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_provenance ;
    np:hasPublicationInfo dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_provenance a np:Provenance .
  dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_assertion {
  miriam-gene:10148 a ncit:C16612 .
  lld:C1961102 a ncit:C7057 .
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}
dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_provenance {
  dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_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 ;
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    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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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 ;
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}
dgn-np:NP837504.RAuNA3OJj0k0o3kHwafYBvZo9xAMQiIw3Wob_2yEL8QJ4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:08+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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}