@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8> .
@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:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_head {
  this: np:hasAssertion dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_assertion ;
    np:hasProvenance dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_provenance ;
    np:hasPublicationInfo dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_assertion a np:Assertion .
  dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_provenance a np:Provenance .
  dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_assertion {
  miriam-gene:79728 a ncit:C16612 .
  lld:C0678222 a ncit:C7057 .
  dgn-gda:DGNd8cf283ec1a95fbaf9419715ca355371 sio:SIO_000628 miriam-gene:79728 , lld:C0678222 ;
    a sio:SIO_001121 .
}
dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_provenance {
  dgn-np:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_assertion dcterms:description "[Since germline mutations in the PALB2 (Partner and Localizer of BRCA2) gene have been identified as breast cancer (BC) susceptibility alleles, the geographical spread and risks associated with PALB2 mutations are subject of intense investigation.]. 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:21165770 ;
    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:NP262008.RAj5FLj1eOBXmlrA6O3OtpPT8C2YOalEIn10ZgwKjtyr8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}