@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM> .
@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/v4.0.0/void/> .

dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_head {
  this: np:hasAssertion dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_assertion;
    np:hasProvenance dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_provenance;
    np:hasPublicationInfo dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_assertion a np:Assertion .
  
  dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_provenance a np:Provenance .
  
  dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C1961102 a ncit:C7057 .
  
  dgn-gda:DGNe98c355433a50211f3bd37eebf19ec08 sio:SIO_000628 miriam-gene:1029, lld:C1961102;
    a sio:SIO_001122 .
}

dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_provenance {
  dgn-np:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_assertion dcterms:description
      "[Using data from a genome-wide association study of 907 individuals with childhood acute lymphoblastic leukemia (cases) and 2,398 controls and with validation in samples totaling 2,386 cases and 2,419 controls, we have shown that common variation at 9p21.3 (rs3731217, intron 1 of CDKN2A) influences acute lymphoblastic leukemia risk (odds ratio = 0.71, P = 3.01 x 10(-11)), irrespective of cell lineage.]. 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:20453839;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP810875.RAgEJ_UfZANltlB2_rY8tHXB017YqXvNv1Ogw0OaWk5xM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:52+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}