@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_head {
  this: np:hasAssertion dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion;
    np:hasProvenance dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_provenance;
    np:hasPublicationInfo dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion a np:Assertion .
  
  dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_provenance a np:Provenance .
  
  dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion {
  miriam-gene:7369 a ncit:C16612 .
  
  lld:C0403447 a ncit:C7057 .
  
  dgn-gda:DGN0ae67be6fbbeb56a3020d8f2dec7f80e sio:SIO_000628 miriam-gene:7369, lld:C0403447;
    a sio:SIO_001122 .
}

dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_provenance {
  dgn-np:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_assertion dcterms:description
      "[In recent genetic association studies, common variants including rs12917707 in the UMOD locus have shown strong evidence of association with eGFR, prevalent and incident chronic kidney disease and uromodulin urinary concentration in general population cohorts.]. 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:22947327;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1010156.RAXu_HnDFfl2XaTl62YNBCgmPoQCeWfRlXXU0zktp4nLc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:23+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}