@prefix semsc: <
http://semanticscience.org/resource/
> .
@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@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 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:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_head
{
this:
np:hasAssertion
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_assertion
;
np:hasProvenance
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_provenance
;
np:hasPublicationInfo
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_assertion
a
np:Assertion
.
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_provenance
a
np:Provenance
.
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_assertion
{
miriam-gene:5443
a
ncit:C16612
.
lld:C0020615
a
ncit:C7057
.
dgn-gda:DGN32bdbc59aa825910596f5a96ac26be82
semsc:SIO_000628
miriam-gene:5443
,
lld:C0020615
;
a
semsc:SIO_001121
.
}
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_provenance
{
dgn-np:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_assertion
dct:description
"[Six patients presented with hypoglycaemia and other evidence of cortisol deficiency between 2.5 and 8 years of age; however, two others became cortisol deficient after initial testing showed normal cortisol responses to ACTH, evidence that the glucocorticoid insufficiency of this syndrome may not be congenital, but may develop as late as the third decade.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
semsc:SIO_000772
miriam-pubmed:1850671
;
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:NP208986.RABipzMpNPCZ5AfJhpt0lE__yczOIMyY1rT_G3sNike80130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:55+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
semsc:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}