@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc> .
@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:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_head {
  this: np:hasAssertion dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion ;
    np:hasProvenance dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_provenance ;
    np:hasPublicationInfo dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion a np:Assertion .
  dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_provenance a np:Provenance .
  dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion {
  miriam-gene:79068 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGNb3d1ba6447de1a29c3c6fe69db3151d1 sio:SIO_000628 miriam-gene:79068 , lld:C0038454 ;
    a sio:SIO_001121 .
}
dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_provenance {
  dgn-np:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_assertion dcterms:description "[In a sample of 8,364 white and 2,083 African American men and women with no clinical history of stroke, significantly greater mean change in performance on the Delayed Word Recall Test was associated with 2 of 4 FTO single nucleotide polymorphisms examined (rs9939609, rs805136, rs17817449, and rs1421085) in whites but not in African Americans (p ≤ 0.002).]. 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:23136261 ;
    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:NP702917.RAHsYAQzbKtPOow0B1JsvR5Vxe6EFmAaHonGfpUHoD-Yc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:07+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> ;
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}