@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc> .
@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:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_head {
  this: np:hasAssertion dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion ;
    np:hasProvenance dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_provenance ;
    np:hasPublicationInfo dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion a np:Assertion .
  dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_provenance a np:Provenance .
  dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion {
  miriam-gene:23047 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGN96299f760089d66e364f39cb8fce1d61 sio:SIO_000628 miriam-gene:23047 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_provenance {
  dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion dcterms:description "[The clinical significance of these findings is indicated by the observation that the BRCA2/APRIN interaction is compromised by BRCA2 missense variants of previously unknown significance and that APRIN expression levels are associated with histological grade in breast cancer and the outcome of breast cancer patients treated with DNA-damaging chemotherapy.]. 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:22293751 ;
    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:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:43+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" .
}