@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk
> .
@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:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_head
{
this:
np:hasAssertion
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion
;
np:hasProvenance
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_provenance
;
np:hasPublicationInfo
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion
a
np:Assertion
.
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_provenance
a
np:Provenance
.
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion
{
miriam-gene:2247
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN14b1690e337391923f6010615777d94e
sio:SIO_000628
miriam-gene:2247
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_provenance
{
dgn-np:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_assertion
dcterms:description
"[This study is to investigate if the FGF2-targeted adenoviral mutant Nijmegen breakage syndrome 1 (FGF2-Ad-NBS1) gene transfer can enhance cisplatin chemosensitisation not only by targeting DNA repair, but also through the induction of antiangiogenesis, whereas at the same time reducing toxicities in treating head and neck squamous cell carcinoma (HNSCC).]. 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:21063405
;
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:NP294263.RACm_Ab7k1J6y7mMfhiKa2RSfxcdps87jfPerDKWbC7Nk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}