@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4> .
@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/v3.0.0/void/> .

dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_head {
  this: np:hasAssertion dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_assertion;
    np:hasProvenance dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_provenance;
    np:hasPublicationInfo dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_assertion a np:Assertion .
  
  dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_provenance a np:Provenance .
  
  dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  
  lld:C0565599 a ncit:C7057 .
  
  dgn-gda:DGNb5e24a89b54a3e0e34bfb45041b5f127 sio:SIO_000628 miriam-gene:342977, lld:C0565599;
    a sio:SIO_001122 .
}

dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_provenance {
  dgn-np:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_assertion dcterms:description
      "[T235 of AGT, C1166 of AT1 and Asp298 of NOS3 were respectively associated with HP, although no significant associations were found between the common genetic variants and HP in ACE, FV, MTHFR, B3AR, TNF-A, PAI-1, GSTP1, mEH, and LPL.]. 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:16369102;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP986186.RAZ9MT-yFipx2RWK72DgQItiDF4RX-FEco1MH5mpvpfg4130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:43+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}