@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw> .
@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:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_head {
  this: np:hasAssertion dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_assertion;
    np:hasProvenance dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_provenance;
    np:hasPublicationInfo dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_assertion a np:Assertion .
  
  dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_provenance a np:Provenance .
  
  dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_assertion {
  miriam-gene:1636 a ncit:C16612 .
  
  lld:C0451718 a ncit:C7057 .
  
  dgn-gda:DGNced155347102113171ecb8053edf070f sio:SIO_000628 miriam-gene:1636, lld:C0451718;
    a sio:SIO_001121 .
}

dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_provenance {
  dgn-np:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_assertion dcterms:description
      "[This study shows that the D allele of ACE gene is closely related to small congenital kidneys with refluxing ureters in patients with primary VUR, and in accordance with previous reports, this allele is also related to the progression of reflux nephropathy.]. 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:11519895;
    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:NP555692.RAeFPsTybJ358UUER3zTNzcsJL7iLrdyRVfFCpOBntabw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}