@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw
> .
@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:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_head
{
this:
np:hasAssertion
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_assertion
;
np:hasProvenance
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_provenance
;
np:hasPublicationInfo
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_assertion
a
np:Assertion
.
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_provenance
a
np:Provenance
.
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_assertion
{
miriam-gene:5992
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN9dee9d0170a7d0ed9be1553bca2c944f
sio:SIO_000628
miriam-gene:5992
,
lld:C0005586
;
a
sio:SIO_001121
.
}
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_provenance
{
dgn-np:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_assertion
dcterms:description
"[The gene encoding the transcription factor RFX4 represents an excellent neurobiological and positional candidate gene for Bipolar disorder due to the potential involvement of RFX4 proteins in the regulation of circadian rhythms and the proximity of the locus to numerous linkage signals on chromosome 12q23.]. 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:15940297
;
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:NP703862.RAI_hwePawuwfw5h95cmHt9vK4w9Ads7agEnryysyeixw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}