@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik> .
@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:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_head {
   this: np:hasAssertion dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_assertion ;
    np:hasProvenance dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_provenance ;
    np:hasPublicationInfo dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_assertion a np:Assertion .
  dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_provenance a np:Provenance .
  dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_assertion {
   miriam-gene:4846 a ncit:C16612 .
  lld:C0002395 a ncit:C7057 .
  dgn-gda:DGN5e82be9d71521fb0973af485f294d574 sio:SIO_000628 miriam-gene:4846 , lld:C0002395 ;
    a sio:SIO_001122 .
}
dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_provenance {
   dgn-np:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_assertion dcterms: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:NP61696.RATHVFj7PpDTn46MaH4N7GMEFAM1Fe2e0I8-oIR2zJ8ik130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:29+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> , <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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}