@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE> .
@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:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_head {
  this: np:hasAssertion dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion;
    np:hasProvenance dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_provenance;
    np:hasPublicationInfo dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion a np:Assertion .
  
  dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_provenance a np:Provenance .
  
  dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGN7fb45fff2b8bd9b23f863a1f72a47840 sio:SIO_000628 miriam-gene:672, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_provenance {
  dgn-np:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_assertion dcterms:description
      "[In 15 of these 22 cases, the relevant history suggestive of hereditary breast cancer and OC (due to BRCA1 or BRCA2 mutations) or Lynch syndrome had been documented, but no action was recorded, and its significance was not appreciated.]. 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:22274317;
    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:NP955753.RAm6AXh1EKP-1Oy9Btk6J84LzCijq7-bhHZnFPH2yPYgE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:58+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" .
}