@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM
> .
@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 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:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_head
{
this:
np:hasAssertion
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion
;
np:hasProvenance
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance
;
np:hasPublicationInfo
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion
a
np:Assertion
.
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance
a
np:Provenance
.
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN32e22a4cb177c44080393b49d11771cf
sio:SIO_000628
miriam-gene:1586
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance
{
dgn-np:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion
dct:description
"[This study suggests that the A2 allele may significantly decrease the overall risk of developing RA. In women, the protective effect of A2 mainly affects the older age group. In men, the clinical severity of RA may decrease in patients with the A2/A2 genotype.]. 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:15235815
;
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:NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}