@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0> .
@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:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_head {
  this: np:hasAssertion dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_assertion;
    np:hasProvenance dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_provenance;
    np:hasPublicationInfo dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_assertion a np:Assertion .
  
  dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_provenance a np:Provenance .
  
  dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_assertion {
  miriam-gene:6097 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN9c05ec51045439cf90a36d6101808f41 sio:SIO_000628 miriam-gene:6097, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_provenance {
  dgn-np:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_assertion dcterms:description
      "[Striking improvements in the understanding of the genetic basis of this autosomal dominant genetic disease are coupled to the understanding of the mechanisms that link the loss of TSC1 (9q34) or TSC2 (16p13.3) genes with the regulation of the Rheb/m-TOR/p70S6K pathway.]. 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:20073603;
    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:NP777449.RAIrTih3hGH9x5_deSovHsIDe1pYt2wLMlIU5X0NGNGV0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:51+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" .
}