@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY> .
@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:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_head {
  this: np:hasAssertion dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion;
    np:hasProvenance dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_provenance;
    np:hasPublicationInfo dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion a np:Assertion .
  
  dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_provenance a np:Provenance .
  
  dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0497327 a ncit:C7057 .
  
  dgn-gda:DGN6705e383b49a1bfb2f4068d91a4ac2c5 sio:SIO_000628 miriam-gene:5663, lld:C0497327;
    a sio:SIO_001122 .
}

dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_provenance {
  dgn-np:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_assertion dcterms:description
      "[ This method provides excellent robustness, speed, and accuracy, and is well suited for determination of the polymorphism in both small and large numbers of samples. This assay could help to overcome the controversy regarding the association between the PS1 s165932 intronic polymorphism and Alzheimer's disease.]. 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:16139258;
    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:NP52625.RA0TkPo0IeWy-WtQgRJGPZdem0G63AWsZ-rQSWGSHkgpY130_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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}