@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE> .
@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:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_head {
   this: np:hasAssertion dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_assertion ;
    np:hasProvenance dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_provenance ;
    np:hasPublicationInfo dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_provenance a np:Provenance .
  dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_assertion {
   miriam-gene:5889 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_provenance {
   dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_assertion dcterms:description "[In addition, in order to resolve whether common RAD51C SNPs are risk factors for breast cancer, we genotyped five tagging single nucleotide polymorphisms, rs12946522, rs304270, rs304283, rs17222691, and rs28363312, all located within the gene, from 993 Finnish breast cancer cases and 871 controls for cancer associated variants.]. 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:21750962 ;
    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 ;
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dgn-np:NP584045.RArdqXwoMedJqQ5cBGtbL-7A1Cv2HU36FKcqz_eq2lnyE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:51+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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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}