@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U> .
@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:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_head {
  this: np:hasAssertion dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_assertion;
    np:hasProvenance dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_provenance;
    np:hasPublicationInfo dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_assertion a np:Assertion .
  
  dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_provenance a np:Provenance .
  
  dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_assertion {
  miriam-gene:7249 a ncit:C16612 .
  
  lld:C1562113 a ncit:C7057 .
  
  dgn-gda:DGN09395f99b4b6cd1582ef47a705cb384a sio:SIO_000628 miriam-gene:7249, lld:C1562113;
    a sio:SIO_001121 .
}

dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_provenance {
  dgn-np:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_assertion dcterms:description
      "[Several sequence alterations were found in the TSC1 and TSC2 genes in both lesional brain tissue and blood of FCD patients, however, in similar frequencies to that of the normal population.]. 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:19175396;
    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:NP796433.RAGiKF_JIuzmPS4w6JHDdc4UnlRCCRR5tLYHDNSuUAx1U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:09+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" .
}