@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4> .
@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:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_head {
  this: np:hasAssertion dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_assertion ;
    np:hasProvenance dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_provenance ;
    np:hasPublicationInfo dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_assertion a np:Assertion .
  dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_provenance a np:Provenance .
  dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_assertion {
  miriam-gene:79728 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
  dgn-gda:DGNd380b3a6943fe8fa4c6ea20302138041 sio:SIO_000628 miriam-gene:79728 , lld:C0006142 ;
    a sio:SIO_001121 .
}
dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_provenance {
  dgn-np:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_assertion dcterms:description "[We screened the PALB2 p.Q775X variant in 71 families with at least three cases of breast cancer (n=48) or breast and ovarian cancers (n=23) that have previously been found negative for at least the most common BRCA1 and BRCA2 mutations reported in the French Canadian population and in 491 women of French Canadian descent who had invasive ovarian cancer and/or low malignant potential tumors of the major histopathological subtypes.]. 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:23302520 ;
    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:NP236329.RANdUDgIGoWfwp9od8_DrVWjyAlYR5OJlihEl3aNupgK4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}