@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg> .
@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:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_head {
  this: np:hasAssertion dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_assertion;
    np:hasProvenance dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_provenance;
    np:hasPublicationInfo dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_assertion a np:Assertion .
  
  dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_provenance a np:Provenance .
  
  dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN72b32403c84b0ed9867a9ff2fc850719 sio:SIO_000628 miriam-gene:1565, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_provenance {
  dgn-np:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_assertion dct:description
      "[In order to elucidate whether a relationship exists between CYP2D6 polymorphism and the risk of developing Alzheimer's disease (AD), CYP2D6 allele and genotype frequencies have been evaluated in 94 patients from Southern Italy (29 men and 65 women, aged 74+/-8 years) with AD, and in 350 healthy controls (204 men, 146 women, aged 33+/-9 years) from the same geographical region.]. 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:16337409;
    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:NP59974.RA1ID3QTvIq8RS5U70VKLlGTjyRze4y1dSdXKHGalGJGg130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+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" .
}