@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic> .
@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:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_head {
  this: np:hasAssertion dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_assertion;
    np:hasProvenance dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_provenance;
    np:hasPublicationInfo dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_assertion a np:Assertion .
  
  dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_provenance a np:Provenance .
  
  dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  
  lld:C0151747 a ncit:C7057 .
  
  dgn-gda:DGN0db670a02fb6d1842280a030fddf2a9e sio:SIO_000628 miriam-gene:5972, lld:C0151747;
    a sio:SIO_001121 .
}

dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_provenance {
  dgn-np:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_assertion dcterms:description
      "[Bartter syndrome, an autosomal recessive renal tubular disorder, is associated with hypokalemic metabolic alkalosis with high renin and aldosterone plasma concentrations with low or normal blood pressure and renal salt loss.]. 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:9502574;
    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:NP661726.RAZw6o_ju9DCxp0DUNyVNJeaaKBZ5IkX5X1OUweXyNAic130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}