@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_head {
   this: np:hasAssertion dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_assertion ;
    np:hasProvenance dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_assertion a np:Assertion .
  dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_provenance a np:Provenance .
  dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_assertion {
   miriam-gene:7249 a ncit:C16612 .
  lld:C0041341 a ncit:C7057 .
  dgn-gda:DGN827535fca794eb8b23dfb1e25e0a2a08 sio:SIO_000628 miriam-gene:7249 , lld:C0041341 ;
    a sio:SIO_001121 .
}
dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_provenance {
   dgn-np:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_assertion dcterms:description "[We have previously described in tuberous sclerosis (TSC) hamartomas the phenomenon of loss of heterozygosity (LOH) for DNA markers in the region of both the TSC2 gene on chromosome 16p13.3 and the TSC1 gene on 9q34.]. 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:8950679 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1363797.RAIV6QxvvncCBtBTNVM9YhUDHoFOpR7QTzOevqjk92L3Y130_publicationInfo {
   this: dcterms:created "2016-05-13T12:52:04+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}