@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ> .
@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:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_head {
  this: np:hasAssertion dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_assertion;
    np:hasProvenance dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_provenance;
    np:hasPublicationInfo dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_assertion a np:Assertion .
  
  dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_provenance a np:Provenance .
  
  dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_assertion {
  miriam-gene:341 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN0c63945e4dbbef9cdc920366b7a896d7 sio:SIO_000628 miriam-gene:341, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_provenance {
  dgn-np:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_assertion dct:description
      "[To identify clinical manifestations and neuropsychological effects of Alzheimer disease (AD) in apolipoprotein (ApoE) e4 carriers and to investigate the relationships between ApoE HhaI polymorphism and apolipoprotein C1 (APOC1) HpaI polymorphism in Taiwanese patients with AD.]. 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:20145290;
    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:NP48340.RAmiN8GiGpMhHLtvAS973zqGqo7TwrTfaG5O025eIpwqQ130_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" .
}