@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4> .
@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:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_head {
  this: np:hasAssertion dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_assertion;
    np:hasProvenance dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_provenance;
    np:hasPublicationInfo dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_assertion a np:Assertion .
  
  dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_provenance a np:Provenance .
  
  dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0442867 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_provenance {
  dgn-np:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_assertion dcterms:description
      "[Germline mutations in PTEN have been found in the majority of cases of sporadic and familial Cowden syndrome (CS), an autosomal dominant inherited cancer syndrome characterised by multiple hamartomas and benign and malignant disease of the thyroid and breast.]. 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:10548886;
    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:NP690453.RAhnrR0PcUGElrQpQom0Hi37pFS3PjgK3xtpnhtf84ek4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}