@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E> .
@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:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_head {
  this: np:hasAssertion dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_assertion ;
    np:hasProvenance dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_provenance ;
    np:hasPublicationInfo dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_assertion a np:Assertion .
  dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_provenance a np:Provenance .
  dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_assertion {
  miriam-gene:1859 a ncit:C16612 .
  lld:C1297882 a ncit:C7057 .
  dgn-gda:DGN265ecd0677c00dedf582d68ca1ad7b1f sio:SIO_000628 miriam-gene:1859 , lld:C1297882 ;
    a sio:SIO_001121 .
}
dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_provenance {
  dgn-np:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_assertion dcterms:description "[To determine the effect of DYRK1A overexpression on BDNF in the genomic context of both complete trisomy 21 and partial trisomy 21, we used lymphoblastoid cell lines from patients with complete aneuploidy of human chromosome 21 (three copies of DYRK1A) and from patients with partial aneuploidy having either two or three copies of DYRK1A.]. 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:22669612 ;
    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:NP661242.RABi5LASYG7fkRn_axm9UvWEPykn5jbkHqW5BDxVAAR7E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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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}