@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck> .
@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/v3.0.0/void/> .

dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_head {
  this: np:hasAssertion dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_assertion;
    np:hasProvenance dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_provenance;
    np:hasPublicationInfo dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_assertion a np:Assertion .
  
  dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_provenance a np:Provenance .
  
  dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  
  lld:C0740394 a ncit:C7057 .
  
  dgn-gda:DGN80d32e13953f730dc4598d663323422d sio:SIO_000628 miriam-gene:5972, lld:C0740394;
    a sio:SIO_001121 .
}

dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_provenance {
  dgn-np:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_assertion dcterms:description
      "[Because all heterozygous REN mutations that have been described are localized in the signal sequence, screening of the REN gene for patients with CKD with hyperuricemia and anemia may best be focused on sequencing of exon 1, which encodes the signal peptide.]. 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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP670054.RAt-m9DUY-dqjbPesKIKl3PXNGTdJCjP3nn3i2nnazkck130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:23+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}