@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_head
{
this:
np:hasAssertion
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_assertion
;
np:hasProvenance
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_assertion
a
np:Assertion
.
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_provenance
a
np:Provenance
.
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_assertion
{
miriam-gene:2908
a
ncit:C16612
.
lld:C0234235
a
ncit:C7057
.
dgn-gda:DGN84e07d15902aefc19ffdd9a649d0902a
sio:SIO_000628
miriam-gene:2908
,
lld:C0234235
;
a
sio:SIO_001121
.
}
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_provenance
{
dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_assertion
dcterms:description
"[The molecular basis of both conditions has been ascribed to mutations in the human glucocorticoid receptor (hGR) gene, which impair the molecular mechanisms of hGR action and alter tissue sensitivity to glucocorticoids.]. 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:23392096
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP435174.RAtoT9xCJpdfXVCZCfi1gxGy84UeY49QoZVfHcAA8js8A130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:54+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
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;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}