@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA> .
@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:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_head {
  this: np:hasAssertion dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_assertion;
    np:hasProvenance dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_provenance;
    np:hasPublicationInfo dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_assertion a np:Assertion .
  
  dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_provenance a np:Provenance .
  
  dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0027765 a ncit:C7057 .
  
  dgn-gda:DGN0b80c42afec868a19b677edc03a885a3 sio:SIO_000628 miriam-gene:7248, lld:C0027765;
    a sio:SIO_001121 .
}

dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_provenance {
  dgn-np:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_assertion dcterms:description
      "[Loss of the tuberous sclerosis complex genes (TSC1 or TSC2) leads to constitutive activation of mTOR and downstream signaling elements, resulting in the development of tumors, neurological disorders, and at the cellular level, severe insulin/IGF-1 resistance.]. 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:18342602;
    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:NP806646.RArJw5EaRRXmiWL7hUnYWHGsWk0mpg9_Im5CgGiBvccrA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:14+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" .
}