@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw
> .
@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/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:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_head
{
this:
np:hasAssertion
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_assertion
;
np:hasProvenance
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_assertion
a
np:Assertion
.
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_provenance
a
np:Provenance
.
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_assertion
{
miriam-gene:1859
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN3c14de43334d173c427da0492e2c5abf
sio:SIO_000628
miriam-gene:1859
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_provenance
{
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_assertion
dcterms:description
"[In human DS LCLs, we confirmed the presence of increased protein levels of DSCR1 and DYRK1A, and showed that the levels of the transcription factor NFATc2 were decreased in DS along with a reduction of its nuclear translocation upon induction of calcium fluxes.]. 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:23830204
;
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 .
}
dgn-np:NP307538.RABVdJaqcyNXfWpu4rEcP8yq3iOquDmS4h9EdabtRjxFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}