@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w> .
@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:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_head {
   this: np:hasAssertion dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_assertion ;
    np:hasProvenance dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_provenance ;
    np:hasPublicationInfo dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_assertion a np:Assertion .
  dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_provenance a np:Provenance .
  dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_assertion {
   miriam-gene:675 a ncit:C16612 .
  lld:C0346153 a ncit:C7057 .
  dgn-gda:DGN30f05983cb336319d841aac294641164 sio:SIO_000628 miriam-gene:675 , lld:C0346153 ;
    a sio:SIO_001121 .
}
dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_provenance {
   dgn-np:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_assertion dcterms:description "[Given that hereditary breast carcinoma is primarily due to germline mutations in one of two breast cancer susceptibility genes, BRCA1 and BRCA2, we have characterised the spectrum of BRCA mutations in a cohort of 37 individuals with early-onset disease (&lt;or=40 years) and no reported family history.]. 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:18431501 ;
    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:NP667417.RAlgfW4jjh7nPr0ASuow5_pfVeg8Gh3X8rIPZBXYXC65w130_publicationInfo {
   this: dcterms:created "2016-05-13T12:46:48+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" .
}