@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU> .
@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:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_head {
  this: np:hasAssertion dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_assertion;
    np:hasProvenance dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_provenance;
    np:hasPublicationInfo dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_assertion a np:Assertion .
  
  dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_provenance a np:Provenance .
  
  dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_assertion {
  miriam-gene:286530 a ncit:C16612 .
  
  lld:C0242596 a ncit:C7057 .
  
  dgn-gda:DGN4c0ee89282cd0460ad0834b26b4a739e sio:SIO_000628 miriam-gene:286530, lld:C0242596;
    a sio:SIO_001122 .
}

dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_provenance {
  dgn-np:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_assertion dcterms:description
      "[As controversy exists regarding the prognostic significance of genomic rearrangements of CRLF2 in pediatric B-precursor acute lymphoblastic leukemia (ALL) classified as standard/intermediate-risk (SR) or high-risk (HR), we assessed the prognostic significance of CRLF2 mRNA expression, CRLF2 genomic lesions (IGH@-CRLF2, P2RY8-CRLF2, CRLF2 F232C), deletion/mutation in genes frequently associated with high CRLF2 expression (IKZF1, JAK, IL7R), and minimal residual disease (MRD) in 1061 pediatric ALL patients (499 HR and 562 SR) on COG Trials P9905/P9906.]. 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:22368272;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP984726.RATpZKBiD-D0Y5lajTYYnc3M3NB7Y29ss3LJ-nXbawKBU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:42+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}