@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg> .
@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:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_head {
  this: np:hasAssertion dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_assertion;
    np:hasProvenance dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_provenance;
    np:hasPublicationInfo dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_assertion a np:Assertion .
  
  dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_provenance a np:Provenance .
  
  dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_assertion {
  miriam-gene:23336 a ncit:C16612 .
  
  lld:C1832526 a ncit:C7057 .
  
  dgn-gda:DGN4be3c32cc743c4e80034ab0538204713 sio:SIO_000628 miriam-gene:23336, lld:C1832526;
    a sio:SIO_001121 .
}

dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_provenance {
  dgn-np:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_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:NP332615.RAbNZGPr7Twoiin5utYM_e4mU3Pfh_N3rjGtjDA-xSppg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:15+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" .
}