@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM> .
@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:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_head {
   this: np:hasAssertion dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_assertion ;
    np:hasProvenance dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_provenance ;
    np:hasPublicationInfo dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_assertion a np:Assertion .
  dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_provenance a np:Provenance .
  dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_assertion {
   miriam-gene:100151664 a ncit:C16612 .
  lld:C0006111 a ncit:C7057 .
  dgn-gda:DGN70be16a16bb2630bc28d4d8a1730cd2d sio:SIO_000628 miriam-gene:100151664 , lld:C0006111 ;
    a sio:SIO_001122 .
}
dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_provenance {
   dgn-np:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_assertion dcterms:description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involved in brain aging, and could be used to replicate observations made in other studies.]. 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:17903297 ;
    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:NP93808.RAP-rDfrm5jC0n-GgXmzXhVhw1_exMF6ObUVURg4P1bHM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:46+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" .
}