@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM> .
@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:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_head {
  this: np:hasAssertion dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_assertion ;
    np:hasProvenance dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_provenance ;
    np:hasPublicationInfo dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_assertion a np:Assertion .
  dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_provenance a np:Provenance .
  dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_assertion {
  miriam-gene:3921 a ncit:C16612 .
  lld:C0011268 a ncit:C7057 .
  dgn-gda:DGN7caedcf4c760f5d794bfdcf9648a5f45 sio:SIO_000628 miriam-gene:3921 , lld:C0011268 ;
    a sio:SIO_001121 .
}
dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_provenance {
  dgn-np:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_assertion dcterms:description "[Using a biallelic genetic marker in exon 3 of LRP, late-onset AD cases markedly differed from the control subjects in the distribution of LRP genotypes, and this difference was highly accentuated among AD cases with positive family history of senile dementia.]. 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:9222170 ;
    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:NP776761.RA_DacL9o8-oBboI_MALU-rs--LUIGzH-tcfeyEGRyEFM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:50+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" .
}