@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU> .
@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:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_head {
  this: np:hasAssertion dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion ;
    np:hasProvenance dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_provenance ;
    np:hasPublicationInfo dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion a np:Assertion .
  dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_provenance a np:Provenance .
  dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  lld:C0595905 a ncit:C7057 .
  dgn-gda:DGN505722fdd97601ef5c1a4d7dc0e59308 sio:SIO_000628 miriam-gene:1437 , lld:C0595905 ;
    a sio:SIO_001121 .
}
dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_provenance {
  dgn-np:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_assertion dcterms:description "[Both AChE-R and AChE-S splice variants as well as several heavier AChE complexes were detected in brain homogenates from the parietal cortex of patients with or without Alzheimer's disease (AD) as well as the cerebrospinal fluid (CSF) of AD patients, compatible with the assumption that CSF AChEs might originate from CNS neurons.]. 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:15009666 ;
    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:NP839988.RAt9qUkdNso18TSH0V3-FWx4f6u8gFtDqtsF14VKnnwkU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:33+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" .
}