@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_head {
  this: np:hasAssertion dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_assertion;
    np:hasProvenance dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_provenance;
    np:hasPublicationInfo dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_assertion a np:Assertion .
  
  dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_provenance a np:Provenance .
  
  dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_assertion {
  miriam-gene:2784 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN0271f06fe8268480317cf9da60c94372 sio:SIO_000628 miriam-gene:2784, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_provenance {
  dgn-np:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_assertion dcterms:description
      "[Furthermore, a latitudinal cline was identified both for the allele frequencies of the SNPs associated with hypertension (CYP3A5, AGT, GNB3), as well as for those associated with the ability to taste phenylthiocarbamide (TAS2R38).]. 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:18248681;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP653708.RAfLD3omidHf2AYwVUfYG4ggd_qgAN47U2EUTH-5C7CbM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:41+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}