@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU> .
@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:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_head {
  this: np:hasAssertion dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion;
    np:hasProvenance dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_provenance;
    np:hasPublicationInfo dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion a np:Assertion .
  
  dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_provenance a np:Provenance .
  
  dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNfd7de3f4aa3ca185fe1a07f5009cacfe sio:SIO_000628 miriam-gene:672, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_provenance {
  dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion dcterms:description
      "[The hereditary breast and ovarian cancer syndrome, primarily due to mutations in BRCA1 and BRCA2, is the main cause of heredity, but also the hereditary nonpolyposis colorectal cancer (HNPCC) syndrome confers an increased risk of ovarian cancer.]. 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:16360201;
    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:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:43+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" .
}