@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_head
{
this:
np:hasAssertion
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion
;
np:hasProvenance
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_provenance
;
np:hasPublicationInfo
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion
a
np:Assertion
.
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_provenance
a
np:Provenance
.
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0035435
a
ncit:C7057
.
dgn-gda:DGNf188ac9c0e3d1a523771561c1e47c5bc
sio:SIO_000628
miriam-gene:4210
,
lld:C0035435
;
a
sio:SIO_001121
.
}
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_provenance
{
dgn-np:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_assertion
dcterms:description
"[These findings suggest that mutations of the MEFV gene may be responsible for rheumatic diseases other than FMF, and patients with JIA especially males, ANA negatives, and ERA subgroups should be screened for MEFV gene mutations in countries where FMF is frequent.]. 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:23588594
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP552574.RAtU0jPOvpRoDfy6ZvTm7lojkFpAr7Nhd1aIg8SNwdIts130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:07+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}