@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk> .
@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:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_head {
  this: np:hasAssertion dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_assertion;
    np:hasProvenance dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_provenance;
    np:hasPublicationInfo dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_assertion a np:Assertion .
  
  dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_provenance a np:Provenance .
  
  dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGN5d6598897b42be35e2bccb020bbc2035 sio:SIO_000628 miriam-gene:5972, lld:C0085580;
    a sio:SIO_001121 .
}

dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_provenance {
  dgn-np:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_assertion dcterms:description
      "[Although these rare monogenic disorders with dramatic phenotypes seem to have little relevance to everyday clinical practice, it is possible that subtle abnormalities of the regulation of the ENaCs may play a role in low-renin forms of 'essential' hypertension.]. 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:9519207;
    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:NP1391564.RA92Ynklsx-P_o6cHl8Jgar-oJTa7_e59rd1yegcu0FKk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:17+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" .
}