@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI> .
@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:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_head {
  this: np:hasAssertion dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion;
    np:hasProvenance dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_provenance;
    np:hasPublicationInfo dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion a np:Assertion .
  
  dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_provenance a np:Provenance .
  
  dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0476089 a ncit:C7057 .
  
  dgn-gda:DGN635846fff4b6edfc219f3505e50ae1a1 sio:SIO_000628 miriam-gene:675, lld:C0476089;
    a sio:SIO_001121 .
}

dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_provenance {
  dgn-np:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_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:NP256228.RAbHTvY9IomGptkGTNoxIMp6LiG3AvQA-LL0vvsWU_QOI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}