@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18> .
@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:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_head {
  this: np:hasAssertion dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion ;
    np:hasProvenance dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_provenance ;
    np:hasPublicationInfo dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion a np:Assertion .
  dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_provenance a np:Provenance .
  dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  lld:C0497327 a ncit:C7057 .
  dgn-gda:DGNcb04f84eb28b38fb9b634b7d32527be8 sio:SIO_000628 miriam-gene:4137 , lld:C0497327 ;
    a sio:SIO_001121 .
}
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_provenance {
  dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion dcterms:description "[The polymorphism of apolipoprotein E (apoE) has been recognized as a genetic risk factor in different neurodegenerative disorders, with or without tau protein- related neuropathology, but few published epidemiological data are available as concerns the association of different apoE alleles with two relatively rare forms of dementia, Pick's disease (PiD) and Huntington's disease (HD).]. 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:10924769 ;
    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:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:57+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" .
}