@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc
> .
@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:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_head
{
this:
np:hasAssertion
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_assertion
;
np:hasProvenance
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_provenance
;
np:hasPublicationInfo
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_assertion
a
np:Assertion
.
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_provenance
a
np:Provenance
.
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0020615
a
ncit:C7057
.
dgn-gda:DGN31c601c15d00ce91695815e05862f4cd
sio:SIO_000628
miriam-gene:3630
,
lld:C0020615
;
a
sio:SIO_001121
.
}
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_provenance
{
dgn-np:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_assertion
dcterms:description
"[We conclude that the heterozygous carriers of the SUR1 mutation had normal glucose metabolism and insulin secretion, indicating that carriers of recessive K(ATP) channel mutations are unlikely to be at an increased risk of hypoglycemia or other disturbances in glucose metabolism.]. 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:11772909
;
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:NP340757.RA-kvEeXsQAFRRGDV7Zi5fx9TLttSA9V0SkQ2fbS3wfXc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:20+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" .
}