@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI> .
@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:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_head {
  this: np:hasAssertion dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_assertion;
    np:hasProvenance dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_provenance;
    np:hasPublicationInfo dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_assertion a np:Assertion .
  
  dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_provenance a np:Provenance .
  
  dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_assertion {
  miriam-gene:285335 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
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dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_provenance {
  dgn-np:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_assertion dcterms:description
      "[The NHE primers and associated polymorphic loci identified in this study can be used in genomic, linkage, and association analysis of NHE genes in future genetic studies of hypertension and renal failure.]. 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:10642288;
    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:NP239707.RAMGmMDxF-hWUraISILwH8YGubWT8_cL8oPAzCW-_fLiI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}