@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA> .
@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:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_head {
  this: np:hasAssertion dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_assertion;
    np:hasProvenance dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_provenance;
    np:hasPublicationInfo dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_assertion a np:Assertion .
  
  dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_provenance a np:Provenance .
  
  dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_assertion {
  miriam-gene:23621 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN5bc7e35a0df6c1debd378aa55093bc3b sio:SIO_000628 miriam-gene:23621, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_provenance {
  dgn-np:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_assertion dct:description
      "[The multifactorial genetic dysfunction in AD includes mutational loci (APP, PS1, PS2) and diverse susceptibility loci (APOE, A2M, AACT, LRP1, IL1A, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3B, NOS3) distributed across the human genome, probably converging in common pathogenic mechanisms that lead to premature neuronal death.]. 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:12452480;
    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:NP47910.RAiDDIVl3XbpI2BRszFgT-pVEypJn136iJvzUVHRVa2AA130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+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" .
}