@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY> .
@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:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_head {
  this: np:hasAssertion dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion ;
    np:hasProvenance dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_provenance ;
    np:hasPublicationInfo dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_provenance a np:Provenance .
  dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion {
  miriam-gene:8301 a ncit:C16612 .
  lld:C0011265 a ncit:C7057 .
  dgn-gda:DGN6233839b8e075afd4638a21d2ce5a4d8 sio:SIO_000628 miriam-gene:8301 , lld:C0011265 ;
    a sio:SIO_001121 .
}
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_provenance {
  dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion dcterms:description "[The associated region extends 120 kb encompassing 11 candidate genes.While AGER encodes a key receptor for amyloid-β protein, an analysis of network context based upon genes now confirmed to contribute to dementia risk (AβPP, PSEN1, PSEN2, CR1, CLU, PICALM, and APOE) suggested strong functional coupling to NOTCH4, with no significant coupling to the remaining candidates.]. 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:21297263 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:18+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> ;
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}