@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg> .
@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:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_head {
  this: np:hasAssertion dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_assertion;
    np:hasProvenance dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_provenance;
    np:hasPublicationInfo dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_assertion a np:Assertion .
  
  dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_provenance a np:Provenance .
  
  dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_assertion {
  miriam-gene:185 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGN2af2a6b9b3bdcc8cf36282108cac7a53 sio:SIO_000628 miriam-gene:185, lld:C0149721;
    a sio:SIO_001122 .
}

dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_provenance {
  dgn-np:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_assertion dct:description
      "[Thus the presence of 1166C allele of AGTR1 and 2350G allele of ACE can be considered as predisposing factors for LVH development in EH. In contrast, association of studied polymorphisms with presence or LVH degree was not detected in patients with arterial hypertension combined with DM2. This may indicate another structure of genetic component of predisposition to LVH in different causes.]. 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:15612584;
    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:NP48806.RAt_62BdHehhrZdjtWUsJtnxJwC_wlrfGw28QFwWB3aMg130_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" .
}