@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ
> .
@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:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_head
{
this:
np:hasAssertion
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_assertion
;
np:hasProvenance
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_assertion
a
np:Assertion
.
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_provenance
a
np:Provenance
.
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0011581
a
ncit:C7057
.
dgn-gda:DGNf129c31f3380ef71082758e70e546fff
sio:SIO_000628
miriam-gene:5972
,
lld:C0011581
;
a
sio:SIO_001121
.
}
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_provenance
{
dgn-np:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_assertion
dcterms:description
"[Given the abundance of the renin-angiotensin system (RAS) components in the brain, their importance in behavior and cognition, and the data that implicates them in the etiology and treatment of depression, it is possible that those RAS gene polymorphisms associated with increased RAS activity may also be associated with depression.]. 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:17499413
;
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:NP604818.RATgXlbl8CHAxzTSFxFjBKPnVzx9FgZVh3A2ll4M_omAQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:03+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" .
}