@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA> .
@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:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_head {
  this: np:hasAssertion dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_assertion;
    np:hasProvenance dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_provenance;
    np:hasPublicationInfo dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_assertion a np:Assertion .
  
  dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_provenance a np:Provenance .
  
  dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_assertion {
  miriam-gene:189 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGN90d394c999b24f1c1e247a06bc9ee06c sio:SIO_000628 miriam-gene:189, lld:C0149721;
    a sio:SIO_001121 .
}

dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_provenance {
  dgn-np:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_assertion dcterms:description
      "[Five genetic polymorphisms of the RAAS (ACE, AGTR1, AGT, CMA, CYP11B2) were analyzed in all patients and the results of genetic analysis were correlated to severity of AS and LVH to determine the importance of the polymorphisms for LVH.]. 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:11275936;
    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:NP187872.RAE12rFOI6GhcJSZy1rIjXugKZP0LJ4rBynXJj8at-PIA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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:disgenetrdf;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}