@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM
> .
@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:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_head
{
this:
np:hasAssertion
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_assertion
;
np:hasProvenance
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_provenance
;
np:hasPublicationInfo
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_assertion
a
np:Assertion
.
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_provenance
a
np:Provenance
.
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0020459
a
ncit:C7057
.
dgn-gda:DGN5b4e6d3d2050f716a9621c8e8040a711
sio:SIO_000628
miriam-gene:3630
,
lld:C0020459
;
a
sio:SIO_001121
.
}
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_provenance
{
dgn-np:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_assertion
dcterms:description
"[Mutant expression resulted in more depolarized membrane potential and elevated insulin secretion at basal glucose concentration (3 mm) compared with cells expressing wild type channels, demonstrating that the inactivation gating defect itself is sufficient to cause loss of channel function and hyperinsulinism.]. 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:18250167
;
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:NP653871.RA9DpS_aobtf-mOgO6_1Vzk9RHeXt5m-5mEWplSqPEtlM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:41+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" .
}