@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw> .
@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:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_head {
  this: np:hasAssertion dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_assertion;
    np:hasProvenance dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_provenance;
    np:hasPublicationInfo dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_assertion a np:Assertion .
  
  dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_provenance a np:Provenance .
  
  dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_assertion {
  miriam-gene:6767 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN6f434b2355594393b27edff3b1ea70f7 sio:SIO_000628 miriam-gene:6767, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_provenance {
  dgn-np:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_assertion dcterms:description
      "[Taken together, our results supported the notion that carriers of 677T or 677TT were at significantly increased risk of developing hypertension and HIP, but indicated caution in interpreting this result, because the study design made marginal significant contribution to the heterogeneity.]. 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:21346782;
    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:NP354092.RA7z5RsEQE_lsQLfN04KwtSvS_h0LSzQuyAxDDSrkiOMw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}