@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0
> .
@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:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_head
{
this:
np:hasAssertion
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_assertion
;
np:hasProvenance
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_provenance
;
np:hasPublicationInfo
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_assertion
a
np:Assertion
.
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_provenance
a
np:Provenance
.
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_assertion
{
miriam-gene:4580
a
ncit:C16612
.
lld:C0553662
a
ncit:C7057
.
dgn-gda:DGN44a7a08e78ab3c5eee233e625426af90
sio:SIO_000628
miriam-gene:4580
,
lld:C0553662
;
a
sio:SIO_001121
.
}
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_provenance
{
dgn-np:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_assertion
dcterms:description
"[To investigate whether methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and erythrocyte concentration of methotrexate (EMTX) could serve as predictors of methotrexate (MTX) efficacy and toxicity in patients with juvenile idiopathic arthritis (JIA).]. 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:20595278
;
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:NP291919.RAxHNetLeaxX0pL6r6BTfAwvd7q6F-O6ENsxl6qoU9ti0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}