@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8> .
@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:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_head {
  this: np:hasAssertion dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion;
    np:hasProvenance dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_provenance;
    np:hasPublicationInfo dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion a np:Assertion .
  
  dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_provenance a np:Provenance .
  
  dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion {
  miriam-gene:4868 a ncit:C16612 .
  
  lld:C0027708 a ncit:C7057 .
  
  dgn-gda:DGNf6ab88c48cd8067878accb9adfe28920 sio:SIO_000628 miriam-gene:4868, lld:C0027708;
    a sio:SIO_001121 .
}

dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_provenance {
  dgn-np:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_assertion dcterms:description
      "[Subsequently, kidneys from patients with congenital nephrotic syndrome of the Finnish type (CNF), presenting with heavy proteinuria, and Wilms' tumor tissue were studied for the corresponding expression pattern for evidence of dedifferentiation/persistence of a fetal expression pattern.]. 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:9438174;
    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:NP535607.RACQXEAlI6vuHf5eTGmr5_6vysIZE3_47ywg5335EYmO8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:23+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" .
}