@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU
> .
@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:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_head
{
this:
np:hasAssertion
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_assertion
;
np:hasProvenance
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_provenance
;
np:hasPublicationInfo
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_assertion
a
np:Assertion
.
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_provenance
a
np:Provenance
.
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_assertion
{
miriam-gene:4729
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGN0bc492a1ef36eb4fac12a2d97acd2061
sio:SIO_000628
miriam-gene:4729
,
lld:C0005586
;
a
sio:SIO_001122
.
}
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_provenance
{
dgn-np:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_assertion
dcterms:description
"[The nuclear-encoded mitochondrial complex I subunit gene, NDUFV2, has been implicated in the pathogenesis of bipolar disorder (BD) in Japanese by virtue of association of variants in its promoter with BD and decreased NDUFV2 messenger ribonucleic acid (mRNA) levels in B lymphoblasts (BLCL) in BD patients compared to controls.]. 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:18199248
;
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:NP53933.RAxR4XtV6_ZCtxe-gpwQI06zfJ5CZ6pwneC9usA_caxTU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}