@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA
> .
@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/
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_assertion
a
np:Assertion
.
dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_provenance
a
np:Provenance
.
dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:4524
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNe54facf292ffc5780a46e15ed5d6dba4
sio:SIO_000628
miriam-gene:4524
,
lld:C0003873
;
a
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.
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dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_provenance
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dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_assertion
dcterms:description
"[Our study suggests that MTHFR C677T and ATIC T675C genotyping combined with clinicopathological data may help to identify patients whom will not benefit from MTX treatment and, therefore, assist clinicians in personalizing RA treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24967362
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP1195765.RACIcdlHhNKaeRYANhpaLJakn1YmvKDpE-Z6-NAExI9UA130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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"v4.0.0" .
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