@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA> .
@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:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_head {
  this: np:hasAssertion dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion ;
    np:hasProvenance dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_provenance ;
    np:hasPublicationInfo dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion a np:Assertion .
  dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_provenance a np:Provenance .
  dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion {
  miriam-gene:10320 a ncit:C16612 .
  lld:C0023452 a ncit:C7057 .
  dgn-gda:DGN6019e09b0182b382f69d8bfffab256f3 sio:SIO_000628 miriam-gene:10320 , lld:C0023452 ;
    a sio:SIO_001121 .
}
dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_provenance {
  dgn-np:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_assertion dcterms:description "[Recent genome-wide association studies (GWAS) that focus on childhood acute lymphoblastic leukemia (ALL), the most common malignancy in children younger than 15 years old, have found evidence that single nucleotide polymorphisms (SNPs) in IKZF1 (7p12.2), ARID5B (10q21.2) and CEBPE (14q11.2) are strongly related to the risk of childhood ALL.]. 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:23608171 ;
    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:NP755927.RATtBuPt1FTNGMc7_darh7CSLLNVQpCxi-u3Kh504r0YA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:38+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" .
}