@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA
> .
@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:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_head
{
this:
np:hasAssertion
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_assertion
;
np:hasProvenance
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_assertion
a
np:Assertion
.
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_provenance
a
np:Provenance
.
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_assertion
{
miriam-gene:10999
a
ncit:C16612
.
lld:C1848140
a
ncit:C7057
.
dgn-gda:DGN0994ec054264f3a0a3754053f9d45d66
sio:SIO_000628
miriam-gene:10999
,
lld:C1848140
;
a
sio:SIO_001121
.
}
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_provenance
{
dgn-np:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_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:NP601057.RAKT6zVtZxYrnMlsYT9hzs3N45Erf8FtG__6o6byhVGaA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}