@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w
> .
@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:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_head
{
this:
np:hasAssertion
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_assertion
;
np:hasProvenance
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_assertion
a
np:Assertion
.
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_provenance
a
np:Provenance
.
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0158981
a
ncit:C7057
.
dgn-gda:DGN38929f701cef36a6dacbbd40669235aa
sio:SIO_000628
miriam-gene:3767
,
lld:C0158981
;
a
sio:SIO_001121
.
}
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_provenance
{
dgn-np:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_assertion
dcterms:description
"[The recent discovery that mutations in the KCNJ11 gene (encoding the Kir6.2 subunit of the K(ATP) channel) are the most common cause of permanent neonatal diabetes, has enabled children to stop insulin injections and achieve improved glycaemic control with high doses of sulphonylurea tablets.]. 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:16925503
;
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:NP223573.RAfNWEVsWi4-ATnHM5MInVAawyEGxBmgnDu0beIN-Ir1w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}