@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_head {
  this: np:hasAssertion dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_assertion;
    np:hasProvenance dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_provenance;
    np:hasPublicationInfo dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_assertion a np:Assertion .
  
  dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_provenance a np:Provenance .
  
  dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_assertion {
  miriam-gene:3356 a ncit:C16612 .
  
  lld:C0033975 a ncit:C7057 .
  
  dgn-gda:DGN08e6c140d15e502c9953a7b788c6b444 sio:SIO_000628 miriam-gene:3356, lld:C0033975;
    a sio:SIO_001122 .
}

dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_provenance {
  dgn-np:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_assertion dcterms:description
      "[ Our data strongly confirm and extend to FAD previous studies suggesting that the genetic variation at this locus is associated with prominent psychotic features in AD and that the 102C allele could play an important role in late-onset AD.]. 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:11566166;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP71460.RAJL8pJ9OlxzfwBh9H6-nX69mECSWA9PezHyw2kcLCYxE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:20+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}