@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY> .
@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:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_head {
  this: np:hasAssertion dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_assertion;
    np:hasProvenance dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_provenance;
    np:hasPublicationInfo dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_assertion a np:Assertion .
  
  dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_provenance a np:Provenance .
  
  dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGN0fec0eacf20d41504d2409c3a58afac7 sio:SIO_000628 miriam-gene:5728, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_provenance {
  dgn-np:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_assertion dcterms: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_literature;
    sio:SIO_000772 miriam-pubmed:12085208;
    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:NP358900.RA77r6f2hziTt92PHdvEmdTl1D1NGxSrvaeI0B3xHJPEY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:28+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" .
}