@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0> .
@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:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_head {
  this: np:hasAssertion dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion;
    np:hasProvenance dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_provenance;
    np:hasPublicationInfo dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion a np:Assertion .
  
  dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_provenance a np:Provenance .
  
  dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion {
  miriam-gene:116085 a ncit:C16612 .
  
  lld:C0392525 a ncit:C7057 .
  
  dgn-gda:DGN316247403309eaaef0e420d2df7687dd sio:SIO_000628 miriam-gene:116085, lld:C0392525;
    a sio:SIO_001121 .
}

dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_provenance {
  dgn-np:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_assertion dcterms:description
      "[This data highlights the importance of the URAT1 renal urate transporter in determining serum urate concentrations and the clinical phenotypes, including nephrolithiasis, that should prompt the clinician to suspect an inherited form of renal hypouricaemia.]. 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:22194875;
    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:NP289942.RAx1ZvbsEsLx2o8lHvX7nn2F83PL1ZuzTZcVpWkshVmM0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}