@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo
> .
@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:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_assertion
;
np:hasProvenance
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_assertion
a
np:Assertion
.
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_provenance
a
np:Provenance
.
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_assertion
{
miriam-gene:3358
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN48541281f0b3baf172ec2efb2cab2f97
sio:SIO_000628
miriam-gene:3358
,
lld:C0007222
;
a
sio:SIO_001121
.
}
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_provenance
{
dgn-np:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_assertion
dcterms:description
"[We conclude that genetic variation in 5HTR2C may be associated with HPA axis activation and stimulated by emotional stress, and also with both psychological and physiological endophenotypes that increase the risk of cardiovascular disease and type-2 diabetes.]. 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:21967853
;
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:NP549857.RAcR1SSS3ONlEVxpl71lhbOu0X-dDd_rKRB-nEiE6LUEo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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
<
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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
"v2.1.0.0" .
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"v2.1.0" .
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