@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8> .
@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:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_head {
  this: np:hasAssertion dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion;
    np:hasProvenance dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_provenance;
    np:hasPublicationInfo dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion a np:Assertion .
  
  dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_provenance a np:Provenance .
  
  dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion {
  miriam-gene:729230 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN4e702c8e57a9107d15927fce5b52e9d5 sio:SIO_000628 miriam-gene:729230, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_provenance {
  dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion dct:description
      "[ These results suggest that two and one genes may be susceptibility loci for hypertension in Japanese men and women, respectively, and that genotyping of these polymorphisms may prove informative for prediction of the genetic risk for 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:15046042;
    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:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+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" .
}