@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4> .
@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:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_head {
  this: np:hasAssertion dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion;
    np:hasProvenance dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance;
    np:hasPublicationInfo dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion a np:Assertion .
  
  dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance a np:Provenance .
  
  dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGNc9a39a6b1dbb2b9e149310bc669f5e17 sio:SIO_000628 miriam-gene:7248, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_provenance {
  dgn-np:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_assertion dcterms:description
      "[While these malformations are believed to result from the effects of TSC1 or TSC2 gene mutations, the molecular mechanisms leading to tuber formation, as well as the onset of seizures, remain largely unknown.]. 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:19912235;
    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:NP775643.RAPmMiUFWPtzQeHP0M4EGNnzZ17A_4TAdqve4Qpd2dNV4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:36+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" .
}