@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM> .
@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/v4.0.0/void/> .

dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_head {
  this: np:hasAssertion dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_assertion;
    np:hasProvenance dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_provenance;
    np:hasPublicationInfo dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_assertion a np:Assertion .
  
  dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_provenance a np:Provenance .
  
  dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_assertion {
  miriam-gene:7249 a ncit:C16612 .
  
  lld:C0086692 a ncit:C7057 .
  
  dgn-gda:DGN2e2f36c1e56bd102cc491058125e490b sio:SIO_000628 miriam-gene:7249, lld:C0086692;
    a sio:SIO_001121 .
}

dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_provenance {
  dgn-np:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_assertion dcterms:description
      "[Inactivating TSC1 and TSC2 mutations cause tuberous sclerosis complex (TSC), an autosomal dominant disorder characterised by the occurrence of benign tumours in various organs and tissues, notably the brain, skin and kidneys.]. 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:24714658;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1171586.RAQ5hd3RJnQxzmfxtLtqABopFcvtHlogvyPCTy3dviwaM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:37+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}