@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o
> .
@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:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_head
{
this:
np:hasAssertion
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion
;
np:hasProvenance
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance
;
np:hasPublicationInfo
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion
a
np:Assertion
.
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance
a
np:Provenance
.
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion
{
miriam-gene:2212
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN77a201706c6ce374b4411fb71caad8e3
sio:SIO_000628
miriam-gene:2212
,
lld:C0024141
;
a
sio:SIO_001122
.
}
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_provenance
{
dgn-np:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_assertion
dct:description
"[ The results of this explorative study support the view that the FcgammaRIIa/IIIa and IIIb polymorphisms constitute factors influencing clinical manifestations and the disease course of SLE but do not represent genetic risk factors for the occurrence of SLE. Higher frequencies of clinical symptoms, haematological and immunological abnormalities as well as an earlier onset of clinical symptoms, haematological and immunological markers of active disease were found in patients with the IIA-R/R131 genotype and the double negative and triple negative genotypes.]. 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:12176802
;
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:NP44102.RAtSlvGTKcMpTrKYfMccc9eMX7sn-BHLQbeiRelvjdw7o130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:20+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" .
}