@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg> .
@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:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_head {
  this: np:hasAssertion dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_assertion;
    np:hasProvenance dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_provenance;
    np:hasPublicationInfo dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_assertion a np:Assertion .
  
  dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_provenance a np:Provenance .
  
  dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN30ee9e065ebdfd101277390a0debe47d sio:SIO_000628 miriam-gene:672, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_provenance {
  dgn-np:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_assertion dcterms:description
      "[After imputation to 1000 Genomes Project data, we assessed associations of 11 million genetic variants with EOC risk from 15,437 cases unselected for family history and 30,845 controls and from 15,252 BRCA1 mutation carriers and 8,211 BRCA2 mutation carriers (3,096 with ovarian cancer), and we combined the results in a meta-analysis.]. 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:25581431;
    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:NP1254795.RAtep-U6wBDHkgoS7-gNuc7k3YcrQ6OFyWAGFzLAZrWeg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:15+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" .
}