@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA
> .
@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:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_head
{
this:
np:hasAssertion
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_assertion
;
np:hasProvenance
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_provenance
;
np:hasPublicationInfo
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_assertion
a
np:Assertion
.
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_provenance
a
np:Provenance
.
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_assertion
{
miriam-gene:267012
a
ncit:C16612
.
lld:C1269683
a
ncit:C7057
.
dgn-gda:DGNc6901fb0259af22637d5ecf0d13a53cf
sio:SIO_000628
miriam-gene:267012
,
lld:C1269683
;
a
sio:SIO_001121
.
}
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_provenance
{
dgn-np:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_assertion
dcterms:description
"[The findings suggest that the DAOA SNPs investigated may not affect MDD or BD phenotype, clinical symptoms or other clinical factors, and are unlikely to be involved in MDD or BD development and treatment outcomes.]. 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:22429365
;
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:NP279197.RAmgnPTRrXVnVrGjcLc8jPN7VIK-kmnFfAnoZkJv2-jSA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}