@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao
> .
@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:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_assertion
a
np:Assertion
.
dgn-np:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_provenance
a
np:Provenance
.
dgn-np:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:1789
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNfa8de7737da7d6880f7b811ddc669ce6
sio:SIO_000628
miriam-gene:1789
,
lld:C0003873
;
a
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.
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dgn-np:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_provenance
{
dgn-np:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_assertion
dcterms:description
"[The objective of this study is to investigate the association between the -283C/T polymorphism at the promotor of DNMT3B gene and susceptibility to rheumatoid arthritis (RA) and to evaluate the effect of the polymorphism on clinical features such as progression of joint destruction in RA.]. 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:19777235
;
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:NP267127.RAbq2utJEO0ecNJ_sFwflZX5ldWX0PfOzUvBVgxqsoAao130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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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pav:authoredBy
<
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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
> ;
pav:version
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