@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58> .
@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:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_head {
   this: np:hasAssertion dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_assertion ;
    np:hasProvenance dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_provenance ;
    np:hasPublicationInfo dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_assertion a np:Assertion .
  dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_provenance a np:Provenance .
  dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_assertion {
   miriam-gene:83990 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGN6d16ded66ee1d0e3a9714140c56172e0 sio:SIO_000628 miriam-gene:83990 , lld:C0006142 ;
    a sio:SIO_001122 .
}
dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_provenance {
   dgn-np:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_assertion dcterms:description "[ Some variants in genes within the base-excision repair pathway (XRCC1) and BRCA1 interacting proteins (BRIP1) may play a role as low penetrance breast cancer risk alleles. Previous association studies of breast cancer and BRCA2 N372H and functional observations for APEX D148E ran counter to our findings of decreased risks. Due to the many comparisons, cautious interpretation and replication of these relationships are warranted.]. 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:15113441 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47722.RAa04YoQpTp8WFmRzSJApiKDMbKXAAn0IqupEvLCFcm58130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:22+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" .
}