@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY
> .
@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:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_head
{
this:
np:hasAssertion
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion
;
np:hasProvenance
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance
;
np:hasPublicationInfo
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion
a
np:Assertion
.
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance
a
np:Provenance
.
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion
{
miriam-gene:1859
a
ncit:C16612
.
lld:C1860787
a
ncit:C7057
.
dgn-gda:DGNb0f2c14af1efac071765ec7ee93a213c
sio:SIO_000628
miriam-gene:1859
,
lld:C1860787
;
a
sio:SIO_001121
.
}
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance
{
dgn-np:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion
dcterms:description
"[Given its localization in both the Down syndrome critical region and in the minimal region for partial monosomy 21, the gene has been studied intensively in animals and in humans, and DYRK1A has been proposed to be involved in the neurodevelopmental alterations associated with these syndromes.]. 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:18405873
;
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:NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:47+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" .
}