@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g
> .
@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:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_head
{
this:
np:hasAssertion
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_assertion
;
np:hasProvenance
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_assertion
a
np:Assertion
.
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_provenance
a
np:Provenance
.
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0158981
a
ncit:C7057
.
dgn-gda:DGN90a17870ad6c9507523e59abc11bc7ac
sio:SIO_000628
miriam-gene:3767
,
lld:C0158981
;
a
sio:SIO_001121
.
}
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_provenance
{
dgn-np:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_assertion
dcterms:description
"[It then considers the molecular mechanism by which gain-of-function mutations in the Kir6.2 subunit of the K(ATP) channel reduce channel inhibition by ATP and thereby lead to neonatal diabetes, and how identification of these mutations has led to changes in therapy.]. 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:16545085
;
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:NP540855.RAG6ors2OJj6IHKk4sgpF9j93lKIj5R0fr-LRu9n7xe2g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:49+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" .
}