@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE> .
@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:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_head {
  this: np:hasAssertion dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion;
    np:hasProvenance dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_provenance;
    np:hasPublicationInfo dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion a np:Assertion .
  
  dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_provenance a np:Provenance .
  
  dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0497327 a ncit:C7057 .
  
  dgn-gda:DGNe9a0d0ef270f6d8d3623e778e0546fa0 sio:SIO_000628 miriam-gene:348, lld:C0497327;
    a sio:SIO_001121 .
}

dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_provenance {
  dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion dcterms:description
      "[We suggest that the lower frequency of dementia in the Amish may be partially explained by the decreased frequency of the APOE-4 allele in this population, and that the inbred nature of this pedigree, with its strong clustering of cases contrasted against the lower frequency of dementia, indicates that additional genetic factors influence late-onset 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:8651641;
    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:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:58+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" .
}