@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os
> .
@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:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_head
{
this:
np:hasAssertion
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_assertion
;
np:hasProvenance
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_provenance
;
np:hasPublicationInfo
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_assertion
a
np:Assertion
.
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_provenance
a
np:Provenance
.
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_assertion
{
miriam-gene:799
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN3468a7d202e8ddb8a7556f2a81a5f5e2
sio:SIO_000628
miriam-gene:799
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_provenance
{
dgn-np:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_assertion
dcterms:description
"[These results suggest that nucleotide excision repair gene polymorphisms, especially in XPC, might potentially be predictive factors for acute toxicity of CRT for bladder cancer, helping individual patient selection for bladder conservation therapy.]. 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:21047201
;
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:NP672928.RA2oxqJFOl-o9ibLPHHF65n6rN2-gskcI3kbI9QlF67os130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}