@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so> .
@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 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:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_head {
  this: np:hasAssertion dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_assertion;
    np:hasProvenance dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_provenance;
    np:hasPublicationInfo dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_assertion a np:Assertion .
  
  dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_provenance a np:Provenance .
  
  dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_assertion {
  miriam-gene:134 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNff56d01c032bf5f7395f7a8d0be95cff sio:SIO_000628 miriam-gene:134, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_provenance {
  dgn-np:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_assertion dct:description
      "[ The adenosine-related gene variants do not appear to alter susceptibility to the disease in this group of essential hypertensives. However, involvement of these genes and the adenosine system cannot be conclusively excluded from essential hypertension pathogenesis as other gene variants may still be involved.]. 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:15257174;
    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:NP49175.RAqZBotvmr6_6e2LdG0_DU34OUHNEcmL6dZ_1BNDei5so130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}