@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI> .
@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:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_head {
  this: np:hasAssertion dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_assertion;
    np:hasProvenance dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_provenance;
    np:hasPublicationInfo dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_assertion a np:Assertion .
  
  dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_provenance a np:Provenance .
  
  dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0086692 a ncit:C7057 .
  
  dgn-gda:DGN7332d8ffcc083dcf253c485772a4b9a0 sio:SIO_000628 miriam-gene:7248, lld:C0086692;
    a sio:SIO_001121 .
}

dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_provenance {
  dgn-np:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_assertion dcterms:description
      "[Tuberous sclerosis (TS), autosomal dominant disorder manifested by the formation of usually benign tumors in the brain, heart, kidneys and skin, results from an inactivating mutation in one of two tumor suppressor genes TSC1 or TSC2.]. 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:17071037;
    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:NP931333.RAyqUPNSjcLpX52uzM8rTMGfeTotMQwZSSf7Dg6y5avYI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:31+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" .
}