@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k> .
@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:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_head {
  this: np:hasAssertion dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion;
    np:hasProvenance dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_provenance;
    np:hasPublicationInfo dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion a np:Assertion .
  
  dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_provenance a np:Provenance .
  
  dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0041341 a ncit:C7057 .
  
  dgn-gda:DGN9fbd2a07ea8b7a0bc93c8c38de15ec38 sio:SIO_000628 miriam-gene:7248, lld:C0041341;
    a sio:SIO_001121 .
}

dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_provenance {
  dgn-np:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_assertion dcterms:description
      "[Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in either the TSC1 or the TSC2 genes and characterized by the development of benign hamartomatous growths in multiple organ systems.]. 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:15888477;
    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:NP494360.RA3zg3urqLJJRDC-C91JkXyDJQ6hgA2Vxt-ggE3gOI54k130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:29+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" .
}