@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM> .
@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:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_head {
  this: np:hasAssertion dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion ;
    np:hasProvenance dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_provenance ;
    np:hasPublicationInfo dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion a np:Assertion .
  dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_provenance a np:Provenance .
  dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion {
  miriam-gene:1161 a ncit:C16612 .
  lld:C0008626 a ncit:C7057 .
  dgn-gda:DGN051ef6478097c04b73943d6452a396fa sio:SIO_000628 miriam-gene:1161 , lld:C0008626 ;
    a sio:SIO_001121 .
}
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_provenance {
  dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion dcterms:description "[We report here cancer risk for cytogenetically tested, healthy subjects with respect to frequency of CAs, CSAs, and CTAs in peripheral blood lymphocytes, using Nordic (1981 subjects with CA data, 1871 subjects with CSA/CTA data) and Italian (1573 subjects with CA data, 877 subjects with CTA/CSA data) cohorts, with a median follow-up of 17 years.]. 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:15026371 ;
    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:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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" .
}