@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY> .
@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:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_head {
   this: np:hasAssertion dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_assertion ;
    np:hasProvenance dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_provenance ;
    np:hasPublicationInfo dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_assertion a np:Assertion .
  dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_provenance a np:Provenance .
  dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_assertion {
   miriam-gene:477 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN38df23cb20eb167eae24b2fe2ad14699 sio:SIO_000628 miriam-gene:477 , lld:C0020538 ;
    a sio:SIO_001122 .
}
dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_provenance {
   dgn-np:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_assertion dct:description "[The rs4961 polymorphism of the ADD1 gene is associated with essential hypertension, but the rs28933400 locus in the ATP1A2 gene may have no association with essential hypertension in the studied 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:19199261 ;
    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:NP47984.RAhHn-NK9vRITfa94-TPOfFNkyxMkXcqP4A08xkFpFfIY130_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" .
}