@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o
> .
@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:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_head
{
this:
np:hasAssertion
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_assertion
;
np:hasProvenance
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_assertion
a
np:Assertion
.
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_provenance
a
np:Provenance
.
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0158981
a
ncit:C7057
.
dgn-gda:DGNe8434bc30804d6079ad8f3366da9f8f4
sio:SIO_000628
miriam-gene:3767
,
lld:C0158981
;
a
sio:SIO_001121
.
}
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_provenance
{
dgn-np:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_assertion
dcterms:description
"[This review focuses on mutations in the pore-forming K(ATP) channel subunit (Kir6.2) that cause neonatal diabetes and discusses recent advances in our understanding of clinical features of neonatal diabetes, its underlying molecular mechanisms and their impact on treatment.]. 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:18566517
;
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:NP677761.RAFOxY-MpzEK9sja8aR6dhfrF8GwUS07BYNW12XSHcY3o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:52+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" .
}