@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w> .
@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:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_head {
  this: np:hasAssertion dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_assertion;
    np:hasProvenance dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_provenance;
    np:hasPublicationInfo dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_assertion a np:Assertion .
  
  dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_provenance a np:Provenance .
  
  dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_assertion {
  miriam-gene:342977 a ncit:C16612 .
  
  lld:C0011265 a ncit:C7057 .
  
  dgn-gda:DGN79a586c439631a53fd7d0156a78c88f0 sio:SIO_000628 miriam-gene:342977, lld:C0011265;
    a sio:SIO_001121 .
}

dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_provenance {
  dgn-np:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_assertion dcterms:description
      "[The multifactorial genetic dysfunction in dementia includes mutational loci (APP, PS1, PS2, TAU) and diverse susceptibility loci (APOE, alpha2M, alphaACT, LRP1, IL1 alpha, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3 beta, NOS3 and many other genes) distributed across the human genome, probably converging in a common pathogenic mechanism that leads to premature neuronal death, in which mitochondrial DNA mutations may contribute to increased genetic variability and heterogeneity.]. 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:16470248;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP535381.RAWg1ar-6NdOPimexpH3O3QLndtIWrzoJ6A1A5D7eQ33w130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:47+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" .
}