@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ> .
@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:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_head {
  this: np:hasAssertion dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion ;
    np:hasProvenance dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion a np:Assertion .
  dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_provenance a np:Provenance .
  dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion {
  miriam-gene:1827 a ncit:C16612 .
  lld:C0013080 a ncit:C7057 .
  dgn-gda:DGN3167c3123cd5f38c81d32d1f1f6f0a45 sio:SIO_000628 miriam-gene:1827 , lld:C0013080 ;
    a sio:SIO_001121 .
}
dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_provenance {
  dgn-np:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_assertion dcterms:description "[Furthermore, the map enabled us to present evidence against the necessary involvement of other loci as well as specific hypotheses that have been put forward in relation to the etiology of DS-i.e., the presence of a single DS consensus region and the sufficiency of DSCR1 and DYRK1A, or APP, in causing several severe DS phenotypes.]. 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:19597142 ;
    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:NP341955.RATp8GVdHQftAvvz4ZyYqDQBRIP3jwhsvr-9yqrAzSnZQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:21+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" .
}