@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0
> .
@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:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_head
{
this:
np:hasAssertion
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_assertion
;
np:hasProvenance
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_provenance
;
np:hasPublicationInfo
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_assertion
a
np:Assertion
.
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_provenance
a
np:Provenance
.
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_assertion
{
miriam-gene:3316
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN2d9f3d6f944b8977e1fbe8d7789aab9d
sio:SIO_000628
miriam-gene:3316
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_provenance
{
dgn-np:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_assertion
dcterms:description
"[Our findings demonstrate for the first time that Hsp27 knockdown enhances the cytotoxic effects of radiotherapy in vivo and provide preclinical proof of principle for clinical trials using Hsp27 antisense technology in the treatment of patients with HNSCC radioresistant cancers.]. 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:19436268
;
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:NP198212.RAnAdJeYBKPRo6lLXAi5r75hTotCv7jqlwEt2A_NPlIs0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:49+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" .
}