@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA> .
@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:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_head {
  this: np:hasAssertion dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion ;
    np:hasProvenance dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_provenance ;
    np:hasPublicationInfo dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion a np:Assertion .
  dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_provenance a np:Provenance .
  dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion {
  miriam-gene:3162 a ncit:C16612 .
  lld:C0085580 a ncit:C7057 .
  dgn-gda:DGN51f264362cb4422d70dc9d421872c8ff sio:SIO_000628 miriam-gene:3162 , lld:C0085580 ;
    a sio:SIO_001121 .
}
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_provenance {
  dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion dcterms:description "[We hypothesized that this gene might be responsible for the variation of susceptibility to essential hypertension (EH) and BP and investigated three polymorphisms in HMOX1 (i.e., the (GT)n repeat in the HMOX1 promoter and single-nucleotide polymorphisms (SNPs) rs2071746 and rs2071749) in population-based samples of 789 Han Chinese from Xinjiang, China.]. 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:21275653 ;
    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:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:04+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" .
}