@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY> .
@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:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_head {
  this: np:hasAssertion dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion;
    np:hasProvenance dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance;
    np:hasPublicationInfo dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion a np:Assertion .
  
  dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance a np:Provenance .
  
  dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion {
  miriam-gene:1282 a ncit:C16612 .
  
  lld:C0085220 a ncit:C7057 .
  
  dgn-gda:DGN83a95114c7bf4618164018302ea48152 sio:SIO_000628 miriam-gene:1282, lld:C0085220;
    a sio:SIO_001121 .
}

dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_provenance {
  dgn-np:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_assertion dcterms:description
      "[The apoE4 targeted replacement mice do not harbor any mutation in the amyloid precursor protein gene and, therefore, are similar to the majority of humans susceptible to cerebral amyloid angiopathy and ICH, where the APOE genetic polymorphism is the only known genetic risk factor.]. 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:18755411;
    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:NP648483.RAOyzsO8c7R8RQhhYmXqXoN8CWDTLesydFZVj9y1lgtMY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:30+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" .
}