@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ
> .
@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:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_head
{
this:
np:hasAssertion
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_assertion
;
np:hasProvenance
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_assertion
a
np:Assertion
.
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_provenance
a
np:Provenance
.
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_assertion
{
miriam-gene:51477
a
ncit:C16612
.
lld:C1848140
a
ncit:C7057
.
dgn-gda:DGNbae72c3d8ab72bb92d648b456df68e7a
sio:SIO_000628
miriam-gene:51477
,
lld:C1848140
;
a
sio:SIO_001121
.
}
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_provenance
{
dgn-np:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_assertion
dcterms:description
"[Previous WS studies have identified functional and structural abnormalities in the hippocampal formation, prefrontal regions crucial for amygdala regulation and social cognition, and the dorsal visual stream, notably the intraparietal sulcus (IPS).]. 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:18308711
;
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:NP868616.RA_IzAqw2jxQYfD6_nEuMKxBwVoxnGYGfW6GjpAybGldQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+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" .
}