@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ> .
@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:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_head {
  this: np:hasAssertion dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion;
    np:hasProvenance dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_provenance;
    np:hasPublicationInfo dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion a np:Assertion .
  
  dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_provenance a np:Provenance .
  
  dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion {
  miriam-gene:6340 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN1492e516989a9f510fb89d20b2595d2f sio:SIO_000628 miriam-gene:6340, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_provenance {
  dgn-np:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_assertion dcterms:description
      "[The roles of these missense mutations in the SCNN1B or SCNN1G gene identified in hypertensive patients are not clear in the pathogenesis of hypertension and the regulation of electrolytes. Thus, further investigation of these mutations, including functional analyses, will be needed.]. 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:15198480;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52088.RATIptUU4YcIQOwtclpHvmFvRPe-EVAT9RgCqKL2xlMXQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}