@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg> .
@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:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_head {
  this: np:hasAssertion dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_assertion;
    np:hasProvenance dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_provenance;
    np:hasPublicationInfo dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_assertion a np:Assertion .
  
  dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_provenance a np:Provenance .
  
  dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0040136 a ncit:C7057 .
  
  dgn-gda:DGN91f5cf374019154a2d8bdb3354957b90 sio:SIO_000628 miriam-gene:5728, lld:C0040136;
    a sio:SIO_001121 .
}

dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_provenance {
  dgn-np:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_assertion dcterms:description
      "[Because the frequency of PTEN suppression in thyroid tumors exceeds that of PTEN mutations or deletions, it is very likely that epigenetic mechanisms, such as promoter hypermethylation, may account for its inactivation in a subset of tumors.]. 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:16487009;
    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:NP205153.RAzymDWwNRo47f954Om13bQBFCq8-MMYCl5Pb3R63cfUg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+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" .
}