@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8> .
@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:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_head {
  this: np:hasAssertion dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_assertion;
    np:hasProvenance dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_provenance;
    np:hasPublicationInfo dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_assertion a np:Assertion .
  
  dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_provenance a np:Provenance .
  
  dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_assertion {
  miriam-gene:1585 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGNa8f142ba26f0e4ac51ebd8706917e938 sio:SIO_000628 miriam-gene:1585, lld:C0149721;
    a sio:SIO_001121 .
}

dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_provenance {
  dgn-np:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_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:NP393382.RAeM7mnOelQuN2-wUn3gV2map_5AxjMb2pzS1BJyfc1f8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:54+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" .
}