@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc> .
@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:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_head {
  this: np:hasAssertion dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion;
    np:hasProvenance dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_provenance;
    np:hasPublicationInfo dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion a np:Assertion .
  
  dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_provenance a np:Provenance .
  
  dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0018552 a ncit:C7057 .
  
  dgn-gda:DGN0d2c5eddde09b0d9bd612f4045f0ab89 sio:SIO_000628 miriam-gene:5728, lld:C0018552;
    a sio:SIO_001121 .
}

dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_provenance {
  dgn-np:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_assertion dcterms:description
      "[Taken together, our findings indicate that benign hamartomas in CD may develop without loss of the second (wild-type) PTEN allele, whereas the pathogenesis of malignant tumours, such as breast carcinomas, appears to require the complete inactivation of Pten as well as further alterations such as the loss of p53-dependent growth control.]. 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:12786840;
    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:NP312756.RAuvHVTHcyQJOZ91FAGpKDAoDIgkXwKbFxYafKn85OEvc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:59+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" .
}