@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI
> .
@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 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:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_head
{
this:
np:hasAssertion
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_assertion
;
np:hasProvenance
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_provenance
;
np:hasPublicationInfo
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_assertion
a
np:Assertion
.
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_provenance
a
np:Provenance
.
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_assertion
{
miriam-gene:2932
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGNb2a891e96cf743f0f70d86d90ab348b8
sio:SIO_000628
miriam-gene:2932
,
lld:C0005586
;
a
sio:SIO_001122
.
}
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_provenance
{
dgn-np:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_assertion
dct:description
"[Results warrant interest for the variants of genes pertaining to the molecular clock as possible endophenotypes of bipolar disorder, but caution ought to be taken in interpreting these preliminary results and future replication studies must be awaited.]. 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:14729229
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43322.RAlAb234vX6OTq8a9BqXaAHxAL-cT3G5w7kv2hc0qj1WI130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}