@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_head
{
this:
np:hasAssertion
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_assertion
;
np:hasProvenance
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_provenance
;
np:hasPublicationInfo
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_assertion
a
np:Assertion
.
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_provenance
a
np:Provenance
.
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C1833104
a
ncit:C7057
.
dgn-gda:DGNccd403f79601843888907389b93c9324
sio:SIO_000628
miriam-gene:3630
,
lld:C1833104
;
a
sio:SIO_001121
.
}
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_provenance
{
dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_assertion
dcterms:description
"[A number of conditions are associated with PNDM, some of which have been elucidated at the molecular levels Among those, the very recently elucidated mutations in KCNJ11 gene, encoding the Kir6.2 subunit of the pancreatic KATP channel involved in regulation of insulin secretion accounts for one third to a half of the PNDM cases.]. 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:16429105
;
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 .
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dgn-np:NP296208.RAEk71LdoIyuGbozgHWbcTw1wsTejPPQWqbWcay0GC5ag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
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