@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM> .
@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:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_head {
  this: np:hasAssertion dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion;
    np:hasProvenance dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_provenance;
    np:hasPublicationInfo dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion a np:Assertion .
  
  dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_provenance a np:Provenance .
  
  dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion {
  miriam-gene:57126 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN44a5726581325e707d6b9a99a99de448 sio:SIO_000628 miriam-gene:57126, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_provenance {
  dgn-np:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_assertion dcterms:description
      "[This sequence, together with the localization of its gene on chromosome 21, suggests that the cerebral amyloid deposited in Alzheimer's disease and aged Down's syndrome is caused by aberrant catabolism of a cell-surface receptor.]. 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:2881207;
    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:NP220194.RAY0uv__vYVaeqP-WxTGf02TpC_rqaVqZU90iZpsHNlcM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+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" .
}