@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo> .
@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:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_head {
  this: np:hasAssertion dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_assertion;
    np:hasProvenance dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_provenance;
    np:hasPublicationInfo dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_assertion a np:Assertion .
  
  dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_provenance a np:Provenance .
  
  dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0085669 a ncit:C7057 .
  
  dgn-gda:DGN64d833840e584a622516499496c917c6 sio:SIO_000628 miriam-gene:2952, lld:C0085669;
    a sio:SIO_001121 .
}

dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_provenance {
  dgn-np:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_assertion dcterms:description
      "[These results suggested that there are no significant associations between the studied genotypes and the risk of developing either form of acute leukemia except GSTT1 null and homozygosity for CYP1A1 genotypes that may play protective roles in the development of ANLL in Turkish children.]. 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:12827651;
    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:NP334229.RADAKaAW78o27QP5KqZcaOY_g5d_evrl8SHctEiYU1pwo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}