@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8> .
@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:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_head {
  this: np:hasAssertion dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_assertion;
    np:hasProvenance dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_provenance;
    np:hasPublicationInfo dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_assertion a np:Assertion .
  
  dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_provenance a np:Provenance .
  
  dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNd14f6e1a278bd0aeb20a93d02e16cd89 sio:SIO_000628 miriam-gene:5663, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_provenance {
  dgn-np:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_assertion dcterms:description
      "[In this study, we tested 27 genes (ACE, BDNF, CH25H, CHRNB2, CST3, CTSD, DAPK1, GALP, hCG2039140, IL1B, LMNA, LOC439999, LOC651924, MAPT, MTHFR, MYH13, PCK1, PGBD1, PRNP, PSEN1, SORCS1, SORL1, TF, TFAM, TNK1, GWA_14q32.13, and GWA_7p15.2), all showing significant association with AD risk in the AlzGene meta-analyses, in a large collection of family-based samples comprised of 4,180 subjects from over 1,300 pedigrees.]. 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:18830724;
    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:NP52616.RAUduTjAK4WsX4AdSH9hni4ViyLTr-ausHAiCkrztxMt8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}