@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_head {
  this: np:hasAssertion dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion;
    np:hasProvenance dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_provenance;
    np:hasPublicationInfo dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion a np:Assertion .
  
  dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_provenance a np:Provenance .
  
  dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNae64f9d5b0aace0e18b9cf9ca41f0652 sio:SIO_000628 miriam-gene:672, lld:C0006826;
    a sio:SIO_001122 .
}

dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_provenance {
  dgn-np:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_assertion dcterms:description
      "[The especially frequent carrier state among the Ashkenazi Jewish population coupled with the high prevalence of BRCA1 and BRCA2 in the same population has led us to search for coinheritance affecting the potential for cancer development.]. 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:15726604;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47779.RAe759MQUw_NiThn3P-l7-ritrTqFr6LAeTwtFYybPREc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}