@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE> .
@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:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_head {
  this: np:hasAssertion dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_assertion;
    np:hasProvenance dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_provenance;
    np:hasPublicationInfo dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_assertion a np:Assertion .
  
  dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_provenance a np:Provenance .
  
  dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGNc545c9635c1763bcbe256321def88a11 sio:SIO_000628 miriam-gene:472, lld:C0024299;
    a sio:SIO_001121 .
}

dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_provenance {
  dgn-np:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_assertion dcterms:description
      "[The association between mutation of the ATM gene and a high incidence of lymphoid malignancy in patients with AT, together with the development of lymphoma in Atm deficient mice, supports the proposal that inactivation of the ATM gene may be of importance in the pathogenesis of sporadic lymphoid malignancy.]. 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:11429421;
    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:NP433099.RAbI1MxKttEtLXuVVcxS_lSqg3UmHFRf35jvsC8UTGXHE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:16+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" .
}