@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA
> .
@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:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_head
{
this:
np:hasAssertion
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_assertion
;
np:hasProvenance
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_provenance
;
np:hasPublicationInfo
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_assertion
a
np:Assertion
.
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_provenance
a
np:Provenance
.
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_assertion
{
miriam-gene:115352
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN78723d9246b8bde24f2c5e2febd5b758
sio:SIO_000628
miriam-gene:115352
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_provenance
{
dgn-np:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_assertion
dcterms:description
"[A promoter polymorphism of FCRL3 (rs7528684) is associated with an increased risk of developing RA in Dutch Caucasians, suggesting that this association is relevant for RA in both Japanese and Caucasian populations.]. 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:17179172
;
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:NP64560.RAQ4umySapJHmtG2bZoaF8fCkerA3B07G9Y_Tb2HC52HA130_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" .
}