@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8
> .
@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/v4.0.0/void/
> .
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_head
{
this:
np:hasAssertion
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_assertion
;
np:hasProvenance
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_assertion
a
np:Assertion
.
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_provenance
a
np:Provenance
.
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_assertion
{
miriam-gene:2908
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN74cf5d76b34fdd432337b196f6b67591
sio:SIO_000628
miriam-gene:2908
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_provenance
{
dgn-np:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_assertion
dcterms:description
"[Excluding noncompliance with GC treatment, abnormal steroid pharmacokinetics, and rare genetic defects in the glucocorticoid receptor (GR), the majority of GC insensitivity in asthma can be attributed to secondary defects related to GR function.]. 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:24162914
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1122690.RAnhvRSBNkmrlCfxqxHaxxmNfSKvShJtn3EZWZKndtBZ8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:15+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}