@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4> .
@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:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_head {
  this: np:hasAssertion dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion;
    np:hasProvenance dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance;
    np:hasPublicationInfo dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion a np:Assertion .
  
  dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance a np:Provenance .
  
  dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0041341 a ncit:C7057 .
  
  dgn-gda:DGN5d0f2ccf3572cdfa74f75f98f509afe3 sio:SIO_000628 miriam-gene:7248, lld:C0041341;
    a sio:SIO_001121 .
}

dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_provenance {
  dgn-np:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_assertion dcterms:description
      "[PEComas are related to the genetic alterations of tuberous sclerosis complex (TSC), an autosomal dominant genetic disease due to losses of TSC1 (9q34) or TSC2 (16p13.3) genes which seem to have a role in the regulation of the Rheb/mTOR/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:18080139;
    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:NP645262.RA9azpQoJiqG6bTrQl_LVZBjIf1FhJF99WScFON1Wo4X4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:38+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" .
}