@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ
> .
@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:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_head
{
this:
np:hasAssertion
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_assertion
;
np:hasProvenance
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_assertion
a
np:Assertion
.
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_provenance
a
np:Provenance
.
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_assertion
{
miriam-gene:3172
a
ncit:C16612
.
lld:C0158981
a
ncit:C7057
.
dgn-gda:DGNed64b4e9812d1184083af7bf1e99c302
sio:SIO_000628
miriam-gene:3172
,
lld:C0158981
;
a
sio:SIO_001121
.
}
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_provenance
{
dgn-np:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_assertion
dcterms:description
"[The knowledge of typical clinical features such as mode of inheritance, age at diagnosis and impaired insulin secretion, as well as genetic testing establishes the diagnosis of MODY, mitochondrial diabetes and neonatal diabetes.]. 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:23037711
;
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:NP1018205.RAHKyhImrPt2GJJ3-U2MrUzXtZlkd0MKqm-GbD0HJztyQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:27+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" .
}