@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8> .
@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:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_head {
  this: np:hasAssertion dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_assertion;
    np:hasProvenance dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_provenance;
    np:hasPublicationInfo dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_assertion a np:Assertion .
  
  dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_provenance a np:Provenance .
  
  dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNc8d802170f2801bb2d0592ba872be9d7 sio:SIO_000628 miriam-gene:183, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_provenance {
  dgn-np:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_assertion dct:description
      "[Our research data showed that the polymorphisms of all the four genes might be associated with hypertension in the Kazakhs group of Xinjiang while there might be interactions existed in AGT, ACE, AGE and CHO.]. 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:19103106;
    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:NP48868.RAnFhu-JYbrqjedfhEyCObPKfH3NWHfy8CrefM7_vnaK8130_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" .
}