@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM> .
@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:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_head {
  this: np:hasAssertion dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_assertion;
    np:hasProvenance dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_provenance;
    np:hasPublicationInfo dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_assertion a np:Assertion .
  
  dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_provenance a np:Provenance .
  
  dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_assertion {
  miriam-gene:5997 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGN29c24f4d41a1e4423139fe5e38781989 sio:SIO_000628 miriam-gene:5997, lld:C0085580;
    a sio:SIO_001121 .
}

dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_provenance {
  dgn-np:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_assertion dcterms:description
      "[This study aimed to explore the individual and interactive effects of five genes from the contractile pathway of VSMC (KCNMB1, RGS2, PRKG, ROCK2, and MYLK) on the risk of essential 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:18496125;
    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:NP800597.RAfK_Vm2yxXAcZ920RQObcysMhXi3jjQOMZoPejYWdxWM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:11+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" .
}