@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8> .
@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:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_head {
  this: np:hasAssertion dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_assertion;
    np:hasProvenance dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_assertion a np:Assertion .
  
  dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_provenance a np:Provenance .
  
  dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_assertion {
  miriam-gene:4287 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGNb779ebd4098935c4e645c74f5ebc322f sio:SIO_000628 miriam-gene:4287, lld:C0085580;
    a sio:SIO_001121 .
}

dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_provenance {
  dgn-np:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_assertion dcterms:description
      "[The present study examined the association of particular human renin gene (REN) and antithrombin III gene (AT3) polymorphisms with essential hypertension by comparing the frequency of specific alleles for each of these genes in 50 hypertensive offspring of hypertensive parents and 91 normotensive offspring of normotensive parents.]. 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:1685742;
    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:NP721234.RA2P760PIynxjUBBD2IgKxbWMHsW0ygEUxN12qrrgmuZ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:18+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" .
}