@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_head {
  this: np:hasAssertion dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_assertion;
    np:hasProvenance dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_provenance;
    np:hasPublicationInfo dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_assertion a np:Assertion .
  
  dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_provenance a np:Provenance .
  
  dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0085400 a ncit:C7057 .
  
  dgn-gda:DGNff8be8a3cd348b339edc04c7433d6dac sio:SIO_000628 miriam-gene:5663, lld:C0085400;
    a sio:SIO_001122 .
}

dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_provenance {
  dgn-np:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_assertion dcterms:description
      "[Some of the PS1 mutations studied (M139V, I143F, G209V, R269H, E280A), but not others, were also associated with faster rates of NFT formation and accelerated neuronal loss in the majority of the patients who harboured them when compared with sporadic Alzheimer's disease patients.]. 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:10468510;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP650688.RAv0LqYx6IlQlQpEgQUBnY_-YXlQTpIdC-1hDPSeo3e_c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:10+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}