@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk
> .
@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:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_head
{
this:
np:hasAssertion
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion
;
np:hasProvenance
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_provenance
;
np:hasPublicationInfo
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion
a
np:Assertion
.
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_provenance
a
np:Provenance
.
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion
{
miriam-gene:7217
a
ncit:C16612
.
lld:C0005586
a
ncit:C7057
.
dgn-gda:DGNc75cdeb42a5084704dcd63177f1f9cb0
sio:SIO_000628
miriam-gene:7217
,
lld:C0005586
;
a
sio:SIO_001122
.
}
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_provenance
{
dgn-np:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_assertion
dcterms:description
"[The 5178C/10398A haplotype in mtDNA may be a risk factor of bipolar disorder (odds ratio, 2.4). Pathophysiological significance of rare mtDNA mutations needs to be verified in the future. This finding may imply the pathophysiological significance of mtDNA in bipolar disorder.]. 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:11223103
;
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:NP62063.RAdZ9CrBofzF3UNcx-X44vNoqpiO53k9lY3YANlt47UDk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}