@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc> .
@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:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_head {
  this: np:hasAssertion dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_assertion ;
    np:hasProvenance dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_provenance ;
    np:hasPublicationInfo dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_provenance a np:Provenance .
  dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_assertion {
  miriam-gene:348 a ncit:C16612 .
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    a sio:SIO_001122 .
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dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_provenance {
  dgn-np:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_assertion dcterms:description "[The objective of our study was thus to determine the allele, genotype, and haplotype frequencies at several single nucleotide polymorphisms (SNPs) in the region of ApoE and test their association with OSA status in children.]. 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:17658295 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP86036.RA_Y38FPiN0viGYJKyD2MrwWwDBW4t8S0OFMAZFjTmsrc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}