@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_head
{
this:
np:hasAssertion
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_assertion
a
np:Assertion
.
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_provenance
a
np:Provenance
.
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_assertion
{
miriam-gene:23158
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN5ae192d07c9d0861afd4231282ff312c
sio:SIO_000628
miriam-gene:23158
,
lld:C0003873
;
a
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.
}
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_provenance
{
dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_assertion
dcterms:description
"[The results from our study suggest that the C3435T MDR1 gene polymorphism may not be related with the RA susceptibility, but may influence the efficacy of RA therapy with DMARDs, and the 3435CC genotype may be related with RRA.]. 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:21947347
;
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 .
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dgn-np:NP631145.RAEm-6gcSdTAGoxFihQKx7RgukDewFh45I_241p0mwk9A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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
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<
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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pav:version
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