@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60
> .
@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:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_assertion
a
np:Assertion
.
dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_provenance
a
np:Provenance
.
dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_publicationInfo
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np:PublicationInfo
.
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dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_assertion
{
miriam-gene:7298
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGNc0d6693a8fb105999023692a4c5ebdfb
sio:SIO_000628
miriam-gene:7298
,
lld:C0023449
;
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.
}
dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_provenance
{
dgn-np:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_assertion
dcterms:description
"[We analysed common genetic polymorphisms of 5,10-methylenetetrahydrofolate reductase (MTHFR), thymidylate synthase (TS), methionine synthase (MS) and methionine synthase reductase (MTRR) in 68 children with ALL and 258 healthy controls to investigate their influence on the risk for ALL.]. 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:17454638
;
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:NP877271.RAgw2ss8JZSygUqJjQG9iqwSf6-V9MIag85CTu416FO60130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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