@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4> .
@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:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_head {
  this: np:hasAssertion dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion ;
    np:hasProvenance dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_provenance ;
    np:hasPublicationInfo dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion a np:Assertion .
  dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_provenance a np:Provenance .
  dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  lld:C0595905 a ncit:C7057 .
  dgn-gda:DGN5c16f2f7f47de4f5926e9d2392b9b484 sio:SIO_000628 miriam-gene:1437 , lld:C0595905 ;
    a sio:SIO_001121 .
}
dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_provenance {
  dgn-np:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_assertion dcterms:description "[This was in contrast to the PSEN1 and APPswe mutation carriers revealing high PiB retention in the cortex and the striatum in combination with abnormal glucose metabolism and CSF biomarkers, and the patients with sAD who showed typically high cortical PiB retention and pathologic CSF levels as well as decreased glucose metabolism when compared with HCs.]. 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:22700814 ;
    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:NP354931.RAfUCVISjw7ofzQmdQwGMXf3yXK7OjoHgfRLEhK0nDC-4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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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}