@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM> .
@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:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_head {
  this: np:hasAssertion dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion ;
    np:hasProvenance dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_provenance ;
    np:hasPublicationInfo dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion a np:Assertion .
  dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_provenance a np:Provenance .
  dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion {
  miriam-gene:3014 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN132d3524df95bed4f9d85070377d79f9 sio:SIO_000628 miriam-gene:3014 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_provenance {
  dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion dcterms:description "[The systematic study of DDR in human tumors and normal tissues by high-throughput tissue microarrays revealed that ATM and gamma-H2AX were engaged in cancer but the extent of their activation was strongly affected by the organ and cell type involved, whereas 53BP1 loss was the most consistent feature among the tumor studied.]. 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:17522062 ;
    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:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:45+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
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}