@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q> .
@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:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_head {
  this: np:hasAssertion dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_assertion;
    np:hasProvenance dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_provenance;
    np:hasPublicationInfo dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_assertion a np:Assertion .
  
  dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_provenance a np:Provenance .
  
  dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0567439 a ncit:C7057 .
  
  dgn-gda:DGNfee338b37fd4c78dc128ed9e3dbbd0c3 sio:SIO_000628 miriam-gene:675, lld:C0567439;
    a sio:SIO_001121 .
}

dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_provenance {
  dgn-np:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_assertion dcterms:description
      "[For gynecologists, knowledge of cancer susceptibility genes such as BRCA1 and BRCA2 and the genetic syndrome hereditary nonpolyposis colorectal cancer (Lynch syndrome II) affects how patients are screened for ovarian and endometrial cancers.]. 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:16582132;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP659121.RAVXTafZSYRJthUXcBFK5Ttxt_vHLsYN49tIyS_CwDl6Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:38+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" .
}