@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_assertion
;
np:hasProvenance
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_provenance
;
np:hasPublicationInfo
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_assertion
a
np:Assertion
.
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_provenance
a
np:Provenance
.
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGN67d3df6f1ba1590d966850b3116b7bb8
sio:SIO_000628
miriam-gene:4210
,
lld:C0021390
;
a
sio:SIO_001121
.
}
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_provenance
{
dgn-np:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_assertion
dcterms:description
"[The results of this study suggest that the MEFV variations may be an additional susceptibility factor for IBD in certain parts of the world where the carrier rate is high, and the genetic background of the IBD patients may show regional changes.]. 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:22810105
;
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:NP549217.RAPLUEgY8L9ne_mTy4jl_9QOU9hThQNRsB-9ke-Teh7dM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
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