@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE> .
@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:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_head {
  this: np:hasAssertion dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion;
    np:hasProvenance dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_provenance;
    np:hasPublicationInfo dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion a np:Assertion .
  
  dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_provenance a np:Provenance .
  
  dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0018552 a ncit:C7057 .
  
  dgn-gda:DGN241f84919306f0ac4f8b4f63df3332b5 sio:SIO_000628 miriam-gene:7248, lld:C0018552;
    a sio:SIO_001121 .
}

dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_provenance {
  dgn-np:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_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-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:NP154886.RA9I4sW1U5WsIdQClvIw66ei1XknBdTSUZrgW2r0r0pmE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}