@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU> .
@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:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_head {
  this: np:hasAssertion dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_assertion;
    np:hasProvenance dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_provenance;
    np:hasPublicationInfo dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_assertion a np:Assertion .
  
  dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_provenance a np:Provenance .
  
  dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_assertion {
  miriam-gene:5664 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGN23ef5f671451d0ce7359b1e66ae4dd10 sio:SIO_000628 miriam-gene:5664, lld:C0162534;
    a sio:SIO_001121 .
}

dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_provenance {
  dgn-np:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_assertion dcterms:description
      "[Mutations in the genes encoding the presenilins (PS1 and PS2) and amyloid precursor protein (APP) are associated with FAD, whereas mutations in the prion protein (PrP) gene are associated with prion disease.]. 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:10631141;
    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:NP890390.RA8H7uZo67l4EfHGmA2ALACnkQ0LHkzafUVZr0px35gzU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:07+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" .
}