@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw> .
@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 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:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_head {
  this: np:hasAssertion dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion;
    np:hasProvenance dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_provenance;
    np:hasPublicationInfo dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion a np:Assertion .
  
  dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_provenance a np:Provenance .
  
  dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN6465dcc27c1771efca22b428aa75c1ba sio:SIO_000628 miriam-gene:5728, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_provenance {
  dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_assertion dct:description
      "[The reported patient, in addition to glioma, had suffered from benign meningioma in the past but did not show any clinical signs of Cowden disease or other hereditary diseases typically associated with PTEN germline mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:12085208;
    prov:wasDerivedFrom dgn-void:ctd_human-20130708;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:ctd_human-20130708 pav:importedOn "2013-07-24"^^xsd:date .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
}

dgn-np:NP27536.RAh3TerZ96AjWjaLxgw08ibKqL86m6ejQtGW8gAv6UUiw130_publicationInfo {
  this: dct:created "2014-10-02T12:32:11+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}