@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI> .
@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:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_head {
   this: np:hasAssertion dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_assertion ;
    np:hasProvenance dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_provenance ;
    np:hasPublicationInfo dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_provenance a np:Provenance .
  dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_assertion {
   miriam-gene:793 a ncit:C16612 .
  lld:C0030567 a ncit:C7057 .
  dgn-gda:DGN5fc93a00b00c6209548ec83df4d108b8 sio:SIO_000628 miriam-gene:793 , lld:C0030567 ;
    a sio:SIO_001121 .
}
dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_provenance {
   dgn-np:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_assertion dcterms:description "[Comparison of diseased human brain tissue with age- and sex-matched controls yielded significant decreases (60-88%) in calbindin protein and mRNA in the substantia nigra (Parkinson disease), in the corpus striatum (Huntington disease), in the nucleus basalis (Alzheimer disease), and in the hippocampus and nucleus raphe dorsalis (Parkinson, Huntington, and Alzheimer diseases) but not in the cerebellum, neocortex, amygdala, or locus ceruleus.]. 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:2140897 ;
    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:NP918293.RAUApIjmaOAxIUYBfDsANA6V32vl6o4aYqI0CNgCFNogI130_publicationInfo {
   this: dcterms:created "2014-10-02T12:41:23+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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    pav:version "v2.1.0.0" .
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}