@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo
> .
@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:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_head
{
this:
np:hasAssertion
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion
;
np:hasProvenance
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_provenance
;
np:hasPublicationInfo
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion
a
np:Assertion
.
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_provenance
a
np:Provenance
.
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion
{
miriam-gene:3359
a
ncit:C16612
.
lld:C0011570
a
ncit:C7057
.
dgn-gda:DGNb50d8553e52b82fad9fe6d839dbf20dc
sio:SIO_000628
miriam-gene:3359
,
lld:C0011570
;
a
sio:SIO_001122
.
}
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_provenance
{
dgn-np:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_assertion
dcterms:description
"[These findings suggest that the HTR3A CC genotype may be associated with alterations in brain structures central to emotion processing, particularly when exposed to stress, and further highlight the potential role of the serotonin system in the pathophysiology of affective disorders. In contrast, those individuals with the T allele, in particular the TT genotype, may be more protected from such alterations combined with minimal exposure to ELS events.]. 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:20694966
;
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:NP86467.RAZhZVs3QJqou3a6zrt2Y-aCAy4aC5O6vKQ83CMde7JOo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}