@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c
> .
@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:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_head
{
this:
np:hasAssertion
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_assertion
;
np:hasProvenance
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_provenance
;
np:hasPublicationInfo
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_assertion
a
np:Assertion
.
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_provenance
a
np:Provenance
.
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_assertion
{
miriam-gene:2908
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN6e79cc4d6c8952dd028aa1f255aabda3
sio:SIO_000628
miriam-gene:2908
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_provenance
{
dgn-np:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_assertion
dcterms:description
"[Subtle changes in glucocorticoid receptor (GR) functioning caused by polymorphisms of the GR gene (NR3C1) may be at the base of the altered reaction of the HPA axis to stress and subsequently related to the development and course of affective disorders.]. 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:19133972
;
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:NP296968.RAUKnLA3Xj_XFhzwsjT16v4XYsmfJ3tt-gnqOzIGphT5c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}