@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho
> .
@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/v4.0.0/void/
> .
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_head
{
this:
np:hasAssertion
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion
;
np:hasProvenance
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance
;
np:hasPublicationInfo
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion
a
np:Assertion
.
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance
a
np:Provenance
.
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGN36d59cde183bb791efe152cc137eed8b
sio:SIO_000628
miriam-gene:4210
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance
{
dgn-np:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion
dcterms:description
"[The results of this study suggest that MEFV gene mutations appear to be an aggravating factor for the severity of RA, and consequently, patients with RA might 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:20031469
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:40+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}