@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc> .
@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:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_head {
  this: np:hasAssertion dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_assertion;
    np:hasProvenance dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_provenance;
    np:hasPublicationInfo dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_assertion a np:Assertion .
  
  dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_provenance a np:Provenance .
  
  dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0005695 a ncit:C7057 .
  
  dgn-gda:DGN5c72f2947602ebfed79e180ef3fdb5ce sio:SIO_000628 miriam-gene:5728, lld:C0005695;
    a sio:SIO_001121 .
}

dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_provenance {
  dgn-np:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_assertion dcterms:description
      "[We examined the pathway components (PIK3CA, PTEN, TSC1, RHEB, and LKB1) and putative upstream regulators (FGFR3 and RAS genes) for mutation, allelic loss, copy number alteration, and expression in bladder tumors and cell lines.]. 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:19789314;
    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:NP784865.RAt_7uJRvu_7utkdtHo8hHGwsEzsjnAhjl3P5rsTkwmwc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:55+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" .
}