@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM> .
@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:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_head {
  this: np:hasAssertion dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_assertion;
    np:hasProvenance dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_provenance;
    np:hasPublicationInfo dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_assertion a np:Assertion .
  
  dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_provenance a np:Provenance .
  
  dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNb6497733daca3264cc2ad5140707ffe3 sio:SIO_000628 miriam-gene:672, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_provenance {
  dgn-np:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_assertion dcterms:description
      "[The high number of women carrying a BRCA1 mutation known to trigger the development of potentially lethal diseases leads us to recommend an offer of genetic counselling and test for the mutation to all females of Inuit origin, thereby hopefully preventing a number of breast and ovarian cancer deaths.]. 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:19504351;
    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:NP743694.RA5scK0iAdQvBERqkGHzLNXpl4Ttke7noX7VH-MJ90ywM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:22+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" .
}