@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto
> .
@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:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_head
{
this:
np:hasAssertion
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_assertion
;
np:hasProvenance
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_provenance
;
np:hasPublicationInfo
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_assertion
a
np:Assertion
.
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_provenance
a
np:Provenance
.
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_assertion
{
miriam-gene:6929
a
ncit:C16612
.
lld:C0043119
a
ncit:C7057
.
dgn-gda:DGN8b14646c933d2adc7feab3442a096232
sio:SIO_000628
miriam-gene:6929
,
lld:C0043119
;
a
sio:SIO_001121
.
}
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_provenance
{
dgn-np:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_assertion
dcterms:description
"[Besides the already known impact of WRN on DNA replication, DNA repair, the p21/p53 pathway, and cell cycle, gene set enrichment analyses of our microarray data also uncover significant impact on the MYC, E2F, cellular E2A and ETV5 transcription factor pathways as well as adipocyte differentiation, HIF1, NFkappaB and IL-6 pathways.]. 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:19502800
;
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:NP488984.RA3Wc8sxUZNxi58usnk5kt6VQq0_ee348drsClYcVJDto130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}