@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw
> .
@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:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_head
{
this:
np:hasAssertion
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_assertion
;
np:hasProvenance
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_assertion
a
np:Assertion
.
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_provenance
a
np:Provenance
.
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_assertion
{
miriam-gene:8988
a
ncit:C16612
.
lld:C1621958
a
ncit:C7057
.
dgn-gda:DGN33d7c08ecf1f2bf80bbdfecd62208a2c
sio:SIO_000628
miriam-gene:8988
,
lld:C1621958
;
a
sio:SIO_001121
.
}
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_provenance
{
dgn-np:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_assertion
dcterms:description
"[The aim of the present study was to investigate whether silencing of Hsp27 or Hsp72 expression in glioblastoma multiforme T98G and anaplastic astrocytoma MOGGCCM cells increases their sensitivity to programmed cell death induction upon temozolomide and/or quercetin treatment.]. 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:24126416
;
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:NP936717.RAShWcVo_D6xfTlo7a5pP61tDH8dt3cFrZXKxeVW5QPFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}