@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA> .
@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:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_head {
  this: np:hasAssertion dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_assertion;
    np:hasProvenance dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_provenance;
    np:hasPublicationInfo dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_assertion a np:Assertion .
  
  dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_provenance a np:Provenance .
  
  dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_assertion {
  miriam-gene:5310 a ncit:C16612 .
  
  lld:C0751674 a ncit:C7057 .
  
  dgn-gda:DGN92af773b5547b63c99a61605c7f90ad4 sio:SIO_000628 miriam-gene:5310, lld:C0751674;
    a sio:SIO_001121 .
}

dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_provenance {
  dgn-np:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_assertion dcterms:description
      "[Diffuse renal LAM lesions are presumed to generate multiple renal cysts by constricting the nephron rather than epithelial hyperplasia obstructing lumina, which is analysis of the TSC genes demonstrated that she did not have TSC2/PKD1 contiguous gene syndrome but had a TSC1 germline mutation (Sato T et al.]. 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:15257730;
    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:NP680684.RAtBPPc4UY5uSaIFKvubdFnLHhICCuVjZTrbEnCn__QBA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:50+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" .
}