@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg
> .
@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:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_head
{
this:
np:hasAssertion
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_assertion
;
np:hasProvenance
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_provenance
;
np:hasPublicationInfo
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_assertion
a
np:Assertion
.
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_provenance
a
np:Provenance
.
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGNd4d59f363ad1875be51e681760ccb2b5
sio:SIO_000628
miriam-gene:4210
,
lld:C0002726
;
a
sio:SIO_001122
.
}
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_provenance
{
dgn-np:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_assertion
dcterms:description
"[We investigated the hypothesis that low-penetrance mutations in genes (TNFRSF1A, MEFV and NALP3/CIAS1) associated with hereditary periodic fever syndromes (HPFs) might be risk factors for AA amyloidosis among patients with chronic inflammatory disorders, including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), Crohn's disease, undiagnosed recurrent fevers and HPFs themselves.]. 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:15071491
;
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:NP54780.RAdiivFgnhKpMgCWJSQ_Ewdk2NKrFH_4sLYSoVXlW-VQg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}