@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY> .
@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:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_head {
   this: np:hasAssertion dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_assertion ;
    np:hasProvenance dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_provenance ;
    np:hasPublicationInfo dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_assertion a np:Assertion .
  dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_provenance a np:Provenance .
  dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_assertion {
   miriam-gene:9365 a ncit:C16612 .
  lld:C1140680 a ncit:C7057 .
  dgn-gda:DGN08568b2c4926c604f57f1c787b739366 sio:SIO_000628 miriam-gene:9365 , lld:C1140680 ;
    a sio:SIO_001121 .
}
dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_provenance {
   dgn-np:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_assertion dcterms:description "[The KL-VS variant was genotyped in women of European ancestry carrying a BRCA mutation: 5,741 BRCA1 mutation carriers (2,997 with breast cancer, 705 with ovarian cancer, and 2,039 cancer free women) and 3,339 BRCA2 mutation carriers (1,846 with breast cancer, 207 with ovarian cancer, and 1,286 cancer free women) from 16 centers.]. 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:22212556 ;
    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:NP217212.RAFNe0EdI-oLnwUTXk4Aa6TsB9ZUzFcZQwWlRNQl513qY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:00+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" .
}