@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc
> .
@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:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_head
{
this:
np:hasAssertion
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_assertion
;
np:hasProvenance
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_provenance
;
np:hasPublicationInfo
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_assertion
a
np:Assertion
.
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_provenance
a
np:Provenance
.
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0004943
a
ncit:C7057
.
dgn-gda:DGN6cecb7fd303da1e1da9d5864991cb631
sio:SIO_000628
miriam-gene:4210
,
lld:C0004943
;
a
sio:SIO_001121
.
}
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_provenance
{
dgn-np:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_assertion
dcterms:description
"[Because the association between MEFV gene mutations and Behçet's disease has been reported before in several studies, we considered that the role of MEFV gene mutations should be studied in patients with RAS, because of the clinical similarities of both diseases.]. 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:23663176
;
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:NP552450.RAdVGyIU7kxYAqeSXf0PJtP2BmP_gjXZJ4h4gSGT3HvWc130_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" .
}