@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_head
{
this:
np:hasAssertion
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion
;
np:hasProvenance
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion
a
np:Assertion
.
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_provenance
a
np:Provenance
.
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0079745
a
ncit:C7057
.
dgn-gda:DGN49b19b40b46e147736c8b8abb866e458
sio:SIO_000628
miriam-gene:4524
,
lld:C0079745
;
a
sio:SIO_001122
.
}
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_provenance
{
dgn-np:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_assertion
dcterms:description
"[The aim of our study was to investigate the potential influence of the C677T and A1298C genetic variants of the methylenetetrahydrofolate reductase (MTHFR) gene on the clinical toxicity and efficacy of MTX in pediatric patients with NHL (n = 95) treated with therapeutic protocols Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) LNH-97 and EURO LB-02.]. 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:23488607
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1060167.RArpaH0sFPv-G-NAJ3_sRP7Ww8JggCr2MpbRsiBMaIAqQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:47+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}