@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10> .
@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/v3.0.0/void/> .

dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_head {
  this: np:hasAssertion dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_assertion;
    np:hasProvenance dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_provenance;
    np:hasPublicationInfo dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_assertion a np:Assertion .
  
  dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_provenance a np:Provenance .
  
  dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0549473 a ncit:C7057 .
  
  dgn-gda:DGNe893a150421be3d45d4ae51c4c6b4c1d sio:SIO_000628 miriam-gene:5728, lld:C0549473;
    a sio:SIO_001121 .
}

dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_provenance {
  dgn-np:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP654720.RAG2VMtPsGm9H-IVwSDGwhG2yt3IzL3qXViE5Rz8vXd10130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:13+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}