@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ> .
@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:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_head {
  this: np:hasAssertion dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_assertion ;
    np:hasProvenance dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_assertion a np:Assertion .
  dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_provenance a np:Provenance .
  dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_assertion {
  miriam-gene:2902 a ncit:C16612 .
  lld:C0002395 a ncit:C7057 .
  dgn-gda:DGN95cc5c04888190a3219b1124d9f264df sio:SIO_000628 miriam-gene:2902 , lld:C0002395 ;
    a sio:SIO_001121 .
}
dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_provenance {
  dgn-np:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_assertion dcterms:description "[Previous work had shown that the ratio of NMDA receptor NR1 subunit mRNA transcripts containing an N-terminal splice cassette to those that do not is markedly lower in regions of the Alzheimer's disease (AD) brain that are susceptible to pathological damage, compared with spared regions in the same cases or homotropic regions in controls.]. 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:15030408 ;
    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:NP476719.RADO2690orkEp9bMDGHLRj9ybv3rLPOqnsg5wvoHXwfQQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:45+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" .
}