@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0> .
@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:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_head {
  this: np:hasAssertion dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion;
    np:hasProvenance dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_provenance;
    np:hasPublicationInfo dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion a np:Assertion .
  
  dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_provenance a np:Provenance .
  
  dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0013182 a ncit:C7057 .
  
  dgn-gda:DGN96f89211e0446652ed29f3da3f696908 sio:SIO_000628 miriam-gene:1565, lld:C0013182;
    a sio:SIO_001122 .
}

dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_provenance {
  dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion dcterms:description
      "[ In this investigation geriatric patients showed a high rate of ADRs. However, no association between the ADR rate and the patients' genotype could be detected, which most likely was a result of the small number of patient samples analysed.Although prophylactic genotyping would have not prevented ADRs in this pilot study, physicians nevertheless have to be aware of potential genetic mutations in patients with polypharmacy.]. 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:15813658;
    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:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}