@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ> .
@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:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_head {
  this: np:hasAssertion dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_assertion;
    np:hasProvenance dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_provenance;
    np:hasPublicationInfo dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_assertion a np:Assertion .
  
  dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_provenance a np:Provenance .
  
  dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_assertion {
  miriam-gene:183 a ncit:C16612 .
  
  lld:C0020456 a ncit:C7057 .
  
  dgn-gda:DGN9f0e8ad8483e60202688fd14a0541171 sio:SIO_000628 miriam-gene:183, lld:C0020456;
    a sio:SIO_001121 .
}

dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_provenance {
  dgn-np:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_assertion dcterms:description
      "[The insertion/deletion (I/D) polymorphism of the angiotensin I-converting enzyme (ACE) gene can modulate risk of nephropathy due to hyperglycemia, and the II genotype (producing low plasma ACE concentrations and probably reduced renal angiotensin II generation and kinin inactivation) may protect against diabetic nephropathy.]. 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:10082486;
    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:NP892432.RAh-q8H9Mzckyrk3r80d4BWxM4sYzMmr51OHY5DXDIWqQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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" .
}