@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg> .
@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:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_head {
  this: np:hasAssertion dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_assertion;
    np:hasProvenance dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_provenance;
    np:hasPublicationInfo dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_assertion a np:Assertion .
  
  dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_provenance a np:Provenance .
  
  dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C1883486 a ncit:C7057 .
  
  dgn-gda:DGNb1d33ed7b21d93d061763eb3ce46da9a sio:SIO_000628 miriam-gene:5728, lld:C1883486;
    a sio:SIO_001121 .
}

dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_provenance {
  dgn-np:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_assertion dcterms:description
      "[Although these data do not preclude the possibility of an increased risk of endometrial cancer in association with the Cowden syndrome, they indicate that germline PTEN mutations do not account for a significant proportion of genetic attributable risk for endometrial carcinoma.]. 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:15589575;
    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:NP472068.RAy1iuak4OU40r9dl-NN96NqZTzC9twxt25hn5vjf6Thg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:18+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" .
}