@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM> .
@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:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_head {
  this: np:hasAssertion dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_assertion ;
    np:hasProvenance dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_provenance ;
    np:hasPublicationInfo dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_assertion a np:Assertion .
  dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_provenance a np:Provenance .
  dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_assertion {
  miriam-gene:23336 a ncit:C16612 .
  lld:C0595905 a ncit:C7057 .
  dgn-gda:DGN3883d3e59c998624a09605b9c00c5e1b sio:SIO_000628 miriam-gene:23336 , lld:C0595905 ;
    a sio:SIO_001121 .
}
dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_provenance {
  dgn-np:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_assertion dcterms:description "[We found that carriers of the KIBRA C-allele demonstrated an increased synchronization in the posterior cingulate cortex (PCC) and medial prefrontal cortex (MPFC) of the DMN and in the right anterior insula, bilateral caudate nuclei, and bilateral dorsal anterior cingulate cortices (dACC) of the ECN compared to individuals with a TT genotype.]. 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:23266749 ;
    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:NP819558.RAIDFIF5x1ndXwMwd0AP2sU0zOrTA3OTnAWWUcZkspQGM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:22+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" .
}