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http://rdf.disgenet.org/nanopublications.trig#NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_assertion
a
np:Assertion
.
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_provenance
a
np:Provenance
.
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:1812
a
ncit:C16612
.
lld:C1839839
a
ncit:C7057
.
dgn-gda:DGN062e89fbf36ec93788cba6a9463efb3e
sio:SIO_000628
miriam-gene:1812
,
lld:C1839839
;
a
sio:SIO_001121
.
}
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_provenance
{
dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_assertion
dcterms:description
"[As the D1 dopamine receptor gene (DRD1) maps to this region and as alterations in dopaminergic neurotransmission have been indirectly implicated in the pathogenesis of MDI, we directly searched for mutations in the coding region of the DRD1 gene in 22 unrelated cases of bipolar I (BPI) disorder derived from multiplex families.]. 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:7485250
;
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 .
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dgn-np:NP598065.RA8Iuf0hVSP1ToiXyzkcs6yqYKifRjjCdDaTzfM4mot1Y130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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
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