@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM> .
@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 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:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_head {
  this: np:hasAssertion dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion;
    np:hasProvenance dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance;
    np:hasPublicationInfo dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion a np:Assertion .
  
  dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance a np:Provenance .
  
  dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_publicationInfo a np:PublicationInfo .
}

dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion {
  miriam-gene:185 a ncit:C16612 .
  
  lld:C0266313 a ncit:C7057 .
  
  dgn-gda:DGNf25d15d63a45277331193e5746ec1c9d sio:SIO_000628 miriam-gene:185, lld:C0266313;
    a sio:SIO_001122 .
}

dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_provenance {
  dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_assertion dc:description
      "[We studied 11 individuals with renal tubular dysgenesis, belonging to nine families, and found that they had homozygous or compound heterozygous mutations in the genes encoding renin, angiotensinogen, angiotensin converting enzyme or angiotensin II receptor type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_curated;
    sio:SIO_000772 miriam-pubmed:16116425;
    prov:wasDerivedFrom dgn-void:uniprot-20130724;
    prov:wasGeneratedBy eco:ECO_0000218 .
  
  dgn-void:source_evidence_curated a eco:ECO_0000205;
    rdfs:comment "Gene-disease associations manually curated."@en;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  
  dgn-void:uniprot-20130724 pav:importedOn "2013-07-24"^^xsd:date .
}

dgn-np:NP248.RAEpWqtnUE6DSiGsVdY88fCfd3vEM5_8bKk5P6QEFU4zM130_publicationInfo {
  this: dc:created "2014-10-02T12:31:58+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}