@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0
> .
@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:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_head
{
this:
np:hasAssertion
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_assertion
;
np:hasProvenance
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_provenance
;
np:hasPublicationInfo
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_assertion
a
np:Assertion
.
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_provenance
a
np:Provenance
.
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN45ec7caca0692aaf028f092e7a1f0233
sio:SIO_000628
miriam-gene:207
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_provenance
{
dgn-np:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_assertion
dcterms:description
"[The established association of the same allelic variant of AKT1 with both cognitive and neuroanatomical aberrations could suggest that AKT1 exerts its effect on verbal learning and memory via neural networks involving prefrontal cortex.]. 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:19051289
;
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:NP784002.RAqWWlkpNCK145JTfys0XqEpHQOzQOUUBfOE_nTDTdHt0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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" .
}