@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8
> .
@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:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_head
{
this:
np:hasAssertion
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion
;
np:hasProvenance
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_provenance
;
np:hasPublicationInfo
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion
a
np:Assertion
.
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_provenance
a
np:Provenance
.
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion
{
miriam-gene:551
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN1030867f00f1431af01ecddae64ae9e2
sio:SIO_000628
miriam-gene:551
,
lld:C0011847
;
a
sio:SIO_001122
.
}
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_provenance
{
dgn-np:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_assertion
dcterms:description
"[ Both mutations result in reduced AVP prohormone processing and secretion probably due to retention in the ER. This supports, at least partly, the hypothesis that the mutations lead to the production of a mutant hormone precursor that fails to fold and/or dimerize properly and, as a consequence, is retained by the ER protein quality control machinery. Perinuclear accumulation of the V67A prohormone outside the ER indicates that additional mechanisms could be involved.]. 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:14678298
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47920.RARVOqZ-MpggFbm_RPIIE15n_KKBQ75ll3YD_bFHjE4_8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}