@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw
> .
@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:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_head
{
this:
np:hasAssertion
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_assertion
;
np:hasProvenance
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_provenance
;
np:hasPublicationInfo
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_assertion
a
np:Assertion
.
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_provenance
a
np:Provenance
.
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0553662
a
ncit:C7057
.
dgn-gda:DGN8ae7163c30a37ea74853589594a28b37
sio:SIO_000628
miriam-gene:4210
,
lld:C0553662
;
a
sio:SIO_001121
.
}
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_provenance
{
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_assertion
dcterms:description
"[Subsequently, it was noticed that patients with certain rheumatic diseases had an increased carrier rate for mutations in the MEFV gene including seronegative spondyloarhtropatheis, Henoch Schönlein purpura, polyarteritis nodosa and some forms of juvenile idiopathic arthritis.]. 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:19796529
;
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 .
}
dgn-np:NP781826.RA6oq97kxpWbjo5QJyNzvu8K7RZYgSV-E3o73gmA36Obw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}