@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE> .
@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:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_head {
  this: np:hasAssertion dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_assertion;
    np:hasProvenance dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_provenance;
    np:hasPublicationInfo dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_assertion a np:Assertion .
  
  dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_provenance a np:Provenance .
  
  dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_assertion {
  miriam-gene:6928 a ncit:C16612 .
  
  lld:C1561643 a ncit:C7057 .
  
  dgn-gda:DGNca42735c0b4dd74c5af684d0f6728f1b sio:SIO_000628 miriam-gene:6928, lld:C1561643;
    a sio:SIO_001121 .
}

dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_provenance {
  dgn-np:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_assertion dcterms:description
      "[We report mutation analysis of the REN gene in 39 kindreds with hyperuricemia and CKD who previously tested negative for mutations in the UMOD (uromodulin) and HNF1B (hepatocyte nuclear factor 1β) genes.]. 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:21903317;
    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:NP289384.RAvOQ2aD4e9ZS5E4i6KIh0D4JS57vtVBXG70_6rhX_nVE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:44+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" .
}