@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8> .
@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:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_head {
  this: np:hasAssertion dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_assertion;
    np:hasProvenance dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_provenance;
    np:hasPublicationInfo dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_assertion a np:Assertion .
  
  dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_provenance a np:Provenance .
  
  dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  
  lld:C0023452 a ncit:C7057 .
  
  dgn-gda:DGN5409209f9daf0b729c8a5b4657879a89 sio:SIO_000628 miriam-gene:8170, lld:C0023452;
    a sio:SIO_001121 .
}

dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_provenance {
  dgn-np:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_assertion dcterms:description
      "[Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression.]. 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:23653000;
    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:NP592019.RAFmLO1V9-qWWbETRPX2ed0OmBYUMiLO_ZF5D4NbAvZK8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:56+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}