@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c
> .
@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:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_head
{
this:
np:hasAssertion
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion
;
np:hasProvenance
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_provenance
;
np:hasPublicationInfo
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion
a
np:Assertion
.
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_provenance
a
np:Provenance
.
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion
{
miriam-gene:3767
a
ncit:C16612
.
lld:C0158981
a
ncit:C7057
.
dgn-gda:DGNeee369ad107a2275f0e86f4990d4e276
sio:SIO_000628
miriam-gene:3767
,
lld:C0158981
;
a
sio:SIO_001121
.
}
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_provenance
{
dgn-np:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_assertion
dcterms:description
"[Our report suggests that screening for KCNJ11 mutations is appropriate in patients diagnosed with neonatal diabetes as it provides valuable information concerning possible course of the disease and choice of 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:20401705
;
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:NP806835.RAVuWVsy2iMPDfKqj7g3k3_TmD8enWRYbeAMTzkS2k07c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:50+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" .
}