@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE> .
@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:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_head {
  this: np:hasAssertion dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_assertion;
    np:hasProvenance dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_provenance;
    np:hasPublicationInfo dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_assertion a np:Assertion .
  
  dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_provenance a np:Provenance .
  
  dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_assertion {
  miriam-gene:7158 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN2d8714a426a7580ee891e44494c35c53 sio:SIO_000628 miriam-gene:7158, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_provenance {
  dgn-np:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_assertion dcterms:description
      "[We also show that very low level of 53BP1 as found in 53BP1 null gliomas or robust 53BP1 gene silencing in glioma cell lines (but not 53BP1 heterozygous tumors or partial gene knockdown) sensitizes glioma cells to ionizing radiation (IR), both in vitro and in vivo.]. 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:22915756;
    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:NP893822.RAq9ASK9vFRfrGPiTyei0fLnjsKrI4__BT4g6HzWUW6oE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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" .
}