@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs
> .
@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:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_head
{
this:
np:hasAssertion
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_assertion
;
np:hasProvenance
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_provenance
;
np:hasPublicationInfo
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_assertion
a
np:Assertion
.
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_provenance
a
np:Provenance
.
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_assertion
{
miriam-gene:57120
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGN9c90476b67af2996c899ab89c3753327
sio:SIO_000628
miriam-gene:57120
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_provenance
{
dgn-np:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_assertion
dcterms:description
"[We investigated a possible association between Kawasaki disease (KD), a systemic vasculitis of unknown etiology, or its coronary artery lesions (CAL) and MEFV gene variants including E148Q, the most common and mild mutation in the MEFV gene for familial Mediterranean fever or vasculitis-related disorders.]. 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:19026701
;
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:NP652833.RATzF2OmP4pvWTvW0Yg8JMtg5qGg6PL0ysUD3G_MiA6fs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}