@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A> .
@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:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_head {
  this: np:hasAssertion dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_assertion ;
    np:hasProvenance dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_provenance ;
    np:hasPublicationInfo dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_assertion a np:Assertion .
  dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_provenance a np:Provenance .
  dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_assertion {
  miriam-gene:10392 a ncit:C16612 .
  lld:C0011615 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_provenance {
  dgn-np:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_assertion dcterms:description "[In order to investigate the role of variation in NLR genes for AD, we genotyped 23 single nucleotide polymorphisms (SNPs) in seven selected NLR genes (CARD4, CARD15, CARD12, NALP1, NALP3, NALP12, MHC2TA) in 392 AD patients and 297 controls by restriction enzyme digestion or TaqMan assays.]. 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:17620097 ;
    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:NP619209.RAIvoGaBuxxuTRTLF8ufyJ_gFxqlVjtXtR3SWaqlQLt0A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:26+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}