@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI> .
@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/v3.0.0/void/> .

dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_head {
  this: np:hasAssertion dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_assertion;
    np:hasProvenance dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_provenance;
    np:hasPublicationInfo dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_assertion a np:Assertion .
  
  dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_provenance a np:Provenance .
  
  dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_assertion {
  miriam-gene:4072 a ncit:C16612 .
  
  lld:C0476089 a ncit:C7057 .
  
  dgn-gda:DGN2c20a96d7301c5c3cf92a72db8620e07 sio:SIO_000628 miriam-gene:4072, lld:C0476089;
    a sio:SIO_001121 .
}

dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_provenance {
  dgn-np:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_assertion dcterms:description
      "[The risk of endometrial cancer in the entire group of EPCAM deletion carriers is significantly lower than that in MSH2 mutation carriers, but the actual risk appears to be dependent on the size and location of the EPCAM deletion.]. 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:23264089;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP542513.RADtCMXg5VtONem_zlkDMle0pXq7aL3j-C9JKvcU-UzzI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:01+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}