@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o
> .
@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:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_head
{
this:
np:hasAssertion
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_assertion
;
np:hasProvenance
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_provenance
;
np:hasPublicationInfo
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_assertion
a
np:Assertion
.
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_provenance
a
np:Provenance
.
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNb7b467769e09626f6c444c493767a4d5
sio:SIO_000628
miriam-gene:4524
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_provenance
{
dgn-np:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_assertion
dcterms:description
"[The results of our study suggest that the MTHFR 677T and 1298C alleles may be associated with an increased rate of RA remission in patients treated with MTX receiving high doses of folic acid supplementation.]. 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:18034620
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP63069.RA68MUKp_E2XkOAhdes8tuggh-8yzFoGMmW3G3I7Aoc6o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}