@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg> .
@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:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_head {
  this: np:hasAssertion dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion;
    np:hasProvenance dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance;
    np:hasPublicationInfo dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion a np:Assertion .
  
  dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance a np:Provenance .
  
  dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion {
  miriam-gene:116372 a ncit:C16612 .
  
  lld:C0018553 a ncit:C7057 .
  
  dgn-gda:DGN80302096f50819ffbff2c3c612fa83de sio:SIO_000628 miriam-gene:116372, lld:C0018553;
    a sio:SIO_001121 .
}

dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_provenance {
  dgn-np:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_assertion dcterms:description
      "[PTEN hamartoma tumour syndrome (PHTS) encompasses several clinical syndromes with germline mutations in the PTEN tumour suppressor gene, including Cowden syndrome which is characterised by an increased risk of breast and thyroid cancers.]. 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:23335809;
    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:NP647851.RAh9IYye1T9VdOJQkqV3OEGQcQQ74C0PiNXy_HLSZAlBg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:30+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" .
}