@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k> .
@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 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:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_head {
  this: np:hasAssertion dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion;
    np:hasProvenance dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_provenance;
    np:hasPublicationInfo dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion a np:Assertion .
  
  dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_provenance a np:Provenance .
  
  dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNe24ff937df0ee5727faea3d0699e5914 sio:SIO_000628 miriam-gene:348, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_provenance {
  dgn-np:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_assertion dct:description
      "[Hippocampal but not amygdalar volumes were associated with presence of one or two APOE epsilon4 alleles in MCI and mild AD, while there was no association of APOE epsilon4 allele with rCBF.]. 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:20541374;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48126.RAgLutXwWU6srsFFng2xopFWDSsdq2FTM_cyagl6izX5k130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}