@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk> .
@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:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_head {
  this: np:hasAssertion dgn-np:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_assertion;
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    np:hasPublicationInfo dgn-np:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_publicationInfo;
    a np:Nanopublication .
  
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dgn-np:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_assertion {
  miriam-gene:286530 a ncit:C16612 .
  
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dgn-np:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_provenance {
  dgn-np:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_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;
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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 .
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dgn-np:NP984721.RA-ZwXZDTu7VXNHZwnlUVbB30In6Zg29ecKhHNVC3alLk130_publicationInfo {
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