@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE> .
@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:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_head {
  this: np:hasAssertion dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_assertion;
    np:hasProvenance dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_provenance;
    np:hasPublicationInfo dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_assertion a np:Assertion .
  
  dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_provenance a np:Provenance .
  
  dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_assertion {
  miriam-gene:3308 a ncit:C16612 .
  
  lld:C0085580 a ncit:C7057 .
  
  dgn-gda:DGN18e250e77671bad8f871f1f6543bfda5 sio:SIO_000628 miriam-gene:3308, lld:C0085580;
    a sio:SIO_001121 .
}

dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_provenance {
  dgn-np:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_assertion dcterms:description
      "[In this study, we focused on five polymorphisms in three genes (HSPA1A, HSPA1B, and HSPA1L) of Hsp70 family to explore the genetic contribution, alone and in combination, of these polymorphisms to essential hypertension risk in a Uygur population.]. 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:19085089;
    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:NP483141.RALShLrk33xt4aPAStYkdeiEXchfoXYCkbU08CCoq2JNE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}