@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ> .
@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 dcterms: <http://purl.org/dc/terms/> .
@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:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_head {
  this: np:hasAssertion dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_assertion ;
    np:hasProvenance dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_assertion a np:Assertion .
  dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_provenance a np:Provenance .
  dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  lld:C0276496 a ncit:C7057 .
  dgn-gda:DGN9ef06e5d4461c2154575d4c3594a958b sio:SIO_000628 miriam-gene:3553 , lld:C0276496 ;
    a sio:SIO_001121 .
}
dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_provenance {
  dgn-np:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_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-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP162271.RAhKYad9HzcXmn3NevQnn2rbJNXa65vqSK7kdXulGwYNQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}