@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00> .
@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:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_head {
  this: np:hasAssertion dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_assertion ;
    np:hasProvenance dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_provenance ;
    np:hasPublicationInfo dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_assertion a np:Assertion .
  dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_provenance a np:Provenance .
  dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_assertion {
  miriam-gene:4830 a ncit:C16612 .
  lld:C0398791 a ncit:C7057 .
  dgn-gda:DGN3309780d95e03c772344af35dcfd1b95 sio:SIO_000628 miriam-gene:4830 , lld:C0398791 ;
    a sio:SIO_001121 .
}
dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_provenance {
  dgn-np:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_assertion dcterms:description "[Cells deficient in ATM (product of the gene that is mutated in ataxia telangiectasia patients) or NBS (product of the gene mutated in the Nijmegen breakage syndrome) show increased yields of both simple and complex chromosomal aberrations after high doses (>0.5Gy) of ionizing radiation (X-rays or γ-rays), however less is known on how these cells respond at low dose.]. 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:21889946 ;
    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:NP451118.RAqrvRiELD35HrtjQoJHgAdjmWLEwboQm-x5rbYVSbT00130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}