@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o> .
@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:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_head {
  this: np:hasAssertion dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion ;
    np:hasProvenance dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_provenance ;
    np:hasPublicationInfo dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion a np:Assertion .
  dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_provenance a np:Provenance .
  dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  lld:C1852467 a ncit:C7057 .
  dgn-gda:DGNd8dc14b6cc609dc242cae8ef32212882 sio:SIO_000628 miriam-gene:3918 , lld:C1852467 ;
    a sio:SIO_001121 .
}
dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_provenance {
  dgn-np:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_assertion dcterms:description "[The increase in CSF levels of lactate dehydrogenase (LDH), glucose-6-phosphate isomerase (G6PI), and fructose-bisphosphate aldolase A (ALDOA) were validated on a larger group of sCJD patients including three possible codon 129 polymorphism carriers and three control groups consisting of nondemented, neurological cases as well as patients suffering from Alzheimer's disease or vascular dementia.]. 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:20866111 ;
    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:NP224798.RAXtR7jvYe6qpPtr0Wuvxhd0FTQWRW105ZY5iu00K1a1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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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}