@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA> .
@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:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_head {
  this: np:hasAssertion dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_assertion;
    np:hasProvenance dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_provenance;
    np:hasPublicationInfo dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_assertion a np:Assertion .
  
  dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_provenance a np:Provenance .
  
  dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0238399 a ncit:C7057 .
  
  dgn-gda:DGN3f3282e41d339ebc48bc3eeee842b0ff sio:SIO_000628 miriam-gene:7248, lld:C0238399;
    a sio:SIO_001121 .
}

dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_provenance {
  dgn-np:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_assertion dcterms:description
      "[Two of the most unusual phenotypes in TSC are the apparent metastasis of benign cells carrying TSC1 and TSC2 mutations, resulting in pulmonary lymphangiomyomatosis, and the ability of cells with TSC1 or TSC2 mutations to differentiate into the separate components of renal angiomyolipomas (vessels, smooth muscle and fat).]. 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:16288294;
    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:NP507142.RABFvfoTyKebrSMvlr41lLPgGJtDLM3dCz-_ICw4ENhDA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:02+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" .
}