@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY> .
@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:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_head {
  this: np:hasAssertion dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion ;
    np:hasProvenance dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_provenance ;
    np:hasPublicationInfo dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion a np:Assertion .
  dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_provenance a np:Provenance .
  dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion {
  miriam-gene:7521 a ncit:C16612 .
  lld:C0004135 a ncit:C7057 .
  dgn-gda:DGNb8c9bede9c67219361e36810debc8757 sio:SIO_000628 miriam-gene:7521 , lld:C0004135 ;
    a sio:SIO_001121 .
}
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_provenance {
  dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion dcterms:description "[In search of functions involved in the regulation of gene amplification, and given the relevance of chromosome breakage in initiating the process, we analyzed the gene amplification ability of cells hypersensitive to inducers of DNA double-strand breaks and defective in cell cycle control: two human fibroblast strains derived from patients affected by ataxia telangiectasia (AT) and two hamster mutant cell lines belonging to complementation group XRCC8 of the rodent X-ray-sensitive mutants.]. 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:11159752 ;
    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:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+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> ;
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}