@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM> .
@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:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_head {
  this: np:hasAssertion dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_assertion;
    np:hasProvenance dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_provenance;
    np:hasPublicationInfo dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_assertion a np:Assertion .
  
  dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_provenance a np:Provenance .
  
  dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_assertion {
  miriam-gene:64109 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGN14306b0b0a8709acc4e4db3c79e63c8c sio:SIO_000628 miriam-gene:64109, lld:C1961102;
    a sio:SIO_001121 .
}

dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_provenance {
  dgn-np:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_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-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:NP501541.RAKBgxheUIUG3LXFAAXH3p_wCUWAl07QsGavEk-np7jDM130_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" .
}