@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w> .
@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:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_head {
  this: np:hasAssertion dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion;
    np:hasProvenance dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_provenance;
    np:hasPublicationInfo dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion a np:Assertion .
  
  dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_provenance a np:Provenance .
  
  dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion {
  miriam-gene:796 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNbef92a12bcede506699eac28489a12c6 sio:SIO_000628 miriam-gene:796, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_provenance {
  dgn-np:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_assertion dcterms:description
      "[The aims of this study were to discover novel polymorphisms or mutations in the 5' flanking region of the human CALCA gene in Japanese subjects and to assess the association between this gene and essential hypertension (EH).]. 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:17485015;
    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:NP63845.RA33ccfAQ86L7qwePbOxACGInvCOqltT_cJMkb3Gxri6w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}