@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8> .
@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:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_head {
  this: np:hasAssertion dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion ;
    np:hasProvenance dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_provenance ;
    np:hasPublicationInfo dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion a np:Assertion .
  dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_provenance a np:Provenance .
  dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion {
  miriam-gene:54209 a ncit:C16612 .
  lld:C0494463 a ncit:C7057 .
  dgn-gda:DGN8402e03f05162391b4ce66f436665758 sio:SIO_000628 miriam-gene:54209 , lld:C0494463 ;
    a sio:SIO_001121 .
}
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_provenance {
  dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion dcterms:description "[The reduced function of TREM2 was speculated to be the main cause in the pathogenic effects of this risk variant, and TREM2 is highly expressed in white matter, as well as in the hippocampus and neocortex, which is partly consistent with the pathological features reported in AD brain, indicating the possible involvement of TREM2 in AD pathogenesis.]. 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:23407992 ;
    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 ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:41+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" .
}