@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo> .
@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:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_head {
  this: np:hasAssertion dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_assertion;
    np:hasProvenance dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_provenance;
    np:hasPublicationInfo dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_assertion a np:Assertion .
  
  dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_provenance a np:Provenance .
  
  dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0085084 a ncit:C7057 .
  
  dgn-gda:DGN12774fe48538d1bdc15ac71d4e8e46cb sio:SIO_000628 miriam-gene:348, lld:C0085084;
    a sio:SIO_001121 .
}

dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_provenance {
  dgn-np:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_assertion dcterms:description
      "[However, no change in the frequency of ApoE alleles was found in two of the clinical and pathological forms of LA (dementia of frontal type and dementia of frontal type with motor neurone disease) although the ApoE E4 allele frequency was elevated in cases of non-fluent progressive aphasia in accordance with the presence of coincidental Alzheimer-type pathological changes.]. 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:7609910;
    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:NP282211.RADErxA_gvG7fR3I3_ZlLBjUaqVZabYu2TUUEcHJ8aEvo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:39+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" .
}