@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU> .
@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:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_head {
   this: np:hasAssertion dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_assertion ;
    np:hasProvenance dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_provenance ;
    np:hasPublicationInfo dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_assertion a np:Assertion .
  dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_provenance a np:Provenance .
  dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_assertion {
   miriam-gene:7248 a ncit:C16612 .
  lld:C0241961 a ncit:C7057 .
  dgn-gda:DGN31a611d147dc6c2156ddd0578c40435f sio:SIO_000628 miriam-gene:7248 , lld:C0241961 ;
    a sio:SIO_001121 .
}
dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_provenance {
   dgn-np:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_assertion dcterms:description "[In this study, 33 patients with FCD (among them 23 with FCD type 2 and 4 patients with multifocal FCD) were investigated (1) clinically as to dermatologic manifestations, retinal hamartoma, cardial rhabdomyoma, and renal angiomyolipoma, and (2) genetically by considering lesional brain tissue and blood using single strand conformation polymorphism (SSCP) electrophoresis and sequencing of the TSC1 and TSC2 genes.]. 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:NP898189.RA6lWPSscEAPdIL00YfIe47YLTgPIEaGd3CgKI_IMOQWU130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:12+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" .
}