@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE> .
@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:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_head {
  this: np:hasAssertion dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_assertion;
    np:hasProvenance dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_provenance;
    np:hasPublicationInfo dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_assertion a np:Assertion .
  
  dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_provenance a np:Provenance .
  
  dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_assertion {
  miriam-gene:1859 a ncit:C16612 .
  
  lld:C1860787 a ncit:C7057 .
  
  dgn-gda:DGNb0f2c14af1efac071765ec7ee93a213c sio:SIO_000628 miriam-gene:1859, lld:C1860787;
    a sio:SIO_001121 .
}

dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_provenance {
  dgn-np:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_assertion dcterms:description
      "[Given its localization in both the Down syndrome critical region and in the minimal region for partial monosomy 21, the gene has been studied intensively in animals and in humans, and DYRK1A has been proposed to be involved in the neurodevelopmental alterations associated with these syndromes.]. 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:18405873;
    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:NP253489.RAcfh63LdjFI2kOVw9e2C-QD9opb2UJ5wIxJKBFfYm5AE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:21+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" .
}