@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI> .
@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:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_head {
  this: np:hasAssertion dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_assertion;
    np:hasProvenance dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_provenance;
    np:hasPublicationInfo dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_assertion a np:Assertion .
  
  dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_provenance a np:Provenance .
  
  dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN729f8d146e823176524daedc1bb824ff sio:SIO_000628 miriam-gene:3553, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_provenance {
  dgn-np:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_assertion dcterms:description
      "[However, although they do not reach statistical significance (which may be due to the relatively restricted number of subjects included in this study), the distribution differences (in normotensives and hypertensives) observed in the cases of EGF and TNF-alpha reflect trends that could be expected from a mechanistic explanation of the pathways that underlie the patho-physiology of 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:12009575;
    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:NP56378.RADnxP5W84veClwmtAvLzq-RdwTVfT4R6hlqCcl_KsXRI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}