@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY> .
@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:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_head {
  this: np:hasAssertion dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_assertion;
    np:hasProvenance dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_provenance;
    np:hasPublicationInfo dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_assertion a np:Assertion .
  
  dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_provenance a np:Provenance .
  
  dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_assertion {
  miriam-gene:7249 a ncit:C16612 .
  
  lld:C0018553 a ncit:C7057 .
  
  dgn-gda:DGN41a3ba548123994571df1f194ec52929 sio:SIO_000628 miriam-gene:7249, lld:C0018553;
    a sio:SIO_001121 .
}

dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_provenance {
  dgn-np:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_assertion dcterms:description
      "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. 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:17013611;
    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:NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:20+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" .
}