@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk
> .
@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:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_head
{
this:
np:hasAssertion
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_assertion
;
np:hasProvenance
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_assertion
a
np:Assertion
.
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_provenance
a
np:Provenance
.
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_assertion
{
miriam-gene:1827
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN2e9e0c624e1c301792bfefa5aca67f8c
sio:SIO_000628
miriam-gene:1827
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_provenance
{
dgn-np:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_assertion
dcterms:description
"[These data provide a mechanism for the reduced cancer incidence in Down's syndrome and identify the calcineurin signalling pathway, and its regulators DSCR1 and DYRK1A, as potential therapeutic targets in cancers arising in all individuals.]. 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:19458618
;
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:NP517034.RANB1SLIknO6KsO5HMkNp0wB1TdnGOPn817XsAALM-GQk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+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" .
}