@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA> .
@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:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_head {
  this: np:hasAssertion dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion;
    np:hasProvenance dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_provenance;
    np:hasPublicationInfo dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion a np:Assertion .
  
  dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_provenance a np:Provenance .
  
  dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion {
  miriam-gene:7249 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN791cc767d0ed0e0eee357fea664da3c7 sio:SIO_000628 miriam-gene:7249, lld:C0022658;
    a sio:SIO_001121 .
}

dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_provenance {
  dgn-np:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_assertion dcterms:description
      "[We conducted a retrospective review of the clinical and radiographic records of 167 patients with tuberous sclerosis to determine the frequency of renal disease, the likelihood of significant renal morbidity, and the effects of genotype (TSC1 vs TSC2) and gender on renal phenotype.]. 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:17003820;
    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:NP527793.RAXSdbQn6AnrbametKqLyu3HwfKPhYM0BC8r7Rp0TevOA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:19+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" .
}