@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k> .
@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:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_head {
  this: np:hasAssertion dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_assertion;
    np:hasProvenance dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_provenance;
    np:hasPublicationInfo dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_assertion a np:Assertion .
  
  dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_provenance a np:Provenance .
  
  dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_assertion {
  miriam-gene:5293 a ncit:C16612 .
  
  lld:C0041341 a ncit:C7057 .
  
  dgn-gda:DGN478d5b183fae01caf16b7c346745281b sio:SIO_000628 miriam-gene:5293, lld:C0041341;
    a sio:SIO_001121 .
}

dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_provenance {
  dgn-np:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_assertion dcterms:description
      "[The collective data discussed have laid the groundwork for important new insights into the many cancers caused by aberrant PI3K activation and the clinically challenging tuberous sclerosis complex disease and have suggested a possible means of treatment for both.]. 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:12773158;
    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:NP255912.RA_aJ0NM9dc_FeyGlHKYNMg_4V4hnsKWEqdlQ8J_p0J4k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:23+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" .
}