@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_assertion
a
np:Assertion
.
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_provenance
a
np:Provenance
.
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0019829
a
ncit:C7057
.
dgn-gda:DGN76222087cece7c157a53dd0162875b27
sio:SIO_000628
miriam-gene:2944
,
lld:C0019829
;
a
sio:SIO_001121
.
}
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_provenance
{
dgn-np:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_assertion
dcterms:description
"[We aimed to validate the impact of GSTT1 and GSTM1 deletions and of the GSTP1Ile105Val polymorphism on outcome and toxicity in 140 patients with advanced Hodgkin's lymphoma enrolled in the prospective multicenter HD2000-GISL trial, comparing ABVD, BEACOPP and CEC regimens.]. 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:21916526
;
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:NP432982.RAEkLKIZOJCtmBNCiq3_reFBDXHr56a6Hwf6RMg7es7ko130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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
<
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> , <
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
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