@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44> .
@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:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_head {
  this: np:hasAssertion dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_assertion;
    np:hasProvenance dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_provenance;
    np:hasPublicationInfo dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_assertion a np:Assertion .
  
  dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_provenance a np:Provenance .
  
  dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0036572 a ncit:C7057 .
  
  dgn-gda:DGNb7e238f67b2dcbc67f9bd2f3ed587e0f sio:SIO_000628 miriam-gene:7248, lld:C0036572;
    a sio:SIO_001121 .
}

dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_provenance {
  dgn-np:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_assertion dcterms:description
      "[The mechanism underlying the association of autism and TSC is as yet unclear but clinical features and neuroimaging investigations suggest that an abnormal TSC gene may directly influence the development of autism rather than it being a secondary effect of seizures or MR.]. 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:9813776;
    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:NP460089.RA8A25ZLlHo7OftPCepGn37bOriT_0UZLlQGpWI_2DG44130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}