@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0> .
@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:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_head {
   this: np:hasAssertion dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_assertion ;
    np:hasProvenance dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_provenance ;
    np:hasPublicationInfo dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_assertion a np:Assertion .
  dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_provenance a np:Provenance .
  dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_assertion {
   miriam-gene:23621 a ncit:C16612 .
  lld:C0497327 a ncit:C7057 .
  dgn-gda:DGN20936b0874d0423a8d3045dbff481414 sio:SIO_000628 miriam-gene:23621 , lld:C0497327 ;
    a sio:SIO_001121 .
}
dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_provenance {
   dgn-np:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_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:NP535378.RANWH7CTiVMr9y9r1G8k1ZLskjTAKIq99I7zeIxx9sYe0130_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" .
}