@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE
> .
@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:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_head
{
this:
np:hasAssertion
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_assertion
;
np:hasProvenance
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_provenance
;
np:hasPublicationInfo
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_assertion
a
np:Assertion
.
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_provenance
a
np:Provenance
.
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_assertion
{
miriam-gene:23336
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN688d7415e54ea49a365475540a2db3d1
sio:SIO_000628
miriam-gene:23336
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_provenance
{
dgn-np:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_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:NP292024.RAANjlb9DU0TvPBP4iakcpRrBBjvp_dDl3vW1TFBHORoE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}