@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_head {
  this: np:hasAssertion dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion ;
    np:hasProvenance dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance ;
    np:hasPublicationInfo dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion a np:Assertion .
  dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance a np:Provenance .
  dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion {
  miriam-gene:672 a ncit:C16612 .
  lld:C0242787 a ncit:C7057 .
  dgn-gda:DGNa51c939112692bb676f161c1e96b2997 sio:SIO_000628 miriam-gene:672 , lld:C0242787 ;
    a sio:SIO_001121 .
}
dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_provenance {
  dgn-np:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_assertion dcterms:description "[Using a TruSeq amplicon cancer panel, this study evaluated 48 familial MBCs (3 BRCA1 germline mutant, 17 BRCA2 germline mutant and 28 BRCAX) for hotspot somatic mutations and copy number changes in 48 common cancer genes.]. 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:25490678 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1246468.RAjSwfJXjgH_s6o0PcYZde67blZnVotFhR-KXx0ndbXLo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:11+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}