@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg> .
@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/v3.0.0/void/> .
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_head {
  this: np:hasAssertion dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion ;
    np:hasProvenance dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_provenance ;
    np:hasPublicationInfo dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion a np:Assertion .
  dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_provenance a np:Provenance .
  dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion {
  miriam-gene:348 a ncit:C16612 .
  lld:C0276496 a ncit:C7057 .
  dgn-gda:DGN3686cc34d4f2297aa0e830838e56f488 sio:SIO_000628 miriam-gene:348 , lld:C0276496 ;
    a sio:SIO_001121 .
}
dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_provenance {
  dgn-np:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_assertion dcterms:description "[For the more common sporadic forms of AD, increased risk has been associated with a number of genes; the most important of which is the epsilon4 allele of apolipoprotein E. Two recent studies, one clinical and one using postmortem material, now show increased risk for AD associated with certain polymorphisms in the genes encoding the alpha and beta isoforms of interleukin-1 (IL-1).]. 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:10850859 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP245937.RAL76CcloNz2wt7gs4ticLJiglnsRkHFEX3GClsNghUJg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:00+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}