@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw
> .
@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:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_head
{
this:
np:hasAssertion
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion
;
np:hasProvenance
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_provenance
;
np:hasPublicationInfo
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion
a
np:Assertion
.
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_provenance
a
np:Provenance
.
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion
{
miriam-gene:3320
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN2ca664afce42cb4c2eeba10671edec98
sio:SIO_000628
miriam-gene:3320
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_provenance
{
dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion
dcterms:description
"[Molecular mechanism of GS unresponsiveness in some patients with multiple sclerosis might be related to increased presence of hsp90 in the GR cytoplasmic complex, leading to the inhibition of GR translocation to nucleus and reduction in its transcription.]. 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:18573821
;
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:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}