@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE> .
@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/v4.0.0/void/> .

dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_head {
  this: np:hasAssertion dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_assertion;
    np:hasProvenance dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_provenance;
    np:hasPublicationInfo dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_assertion a np:Assertion .
  
  dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_provenance a np:Provenance .
  
  dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0276496 a ncit:C7057 .
  
  dgn-gda:DGN4fa53f9cf36261274d5a28ed16a039fd sio:SIO_000628 miriam-gene:5663, lld:C0276496;
    a sio:SIO_001122 .
}

dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_provenance {
  dgn-np:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_assertion dcterms:description
      "[Twenty-one unrelated patients with a history of suspected familial Alzheimer disease (FAD) were screened for mutations in PSEN1, PSEN2, and APP, the known FAD genes encoding the presenilins (PS1 and PS2) and the amyloid precursor protein (APP).]. 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:15776278;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP486030.RAG4pJQiOlBUf0tx_Vwh3f6YpDK3jZ15JQGQo9oXwpfeE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:25+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}