@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU
> .
@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:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_head
{
this:
np:hasAssertion
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion
;
np:hasProvenance
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_provenance
;
np:hasPublicationInfo
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion
a
np:Assertion
.
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_provenance
a
np:Provenance
.
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGNe06207d49735beac628218f864b4d81f
sio:SIO_000628
miriam-gene:4210
,
lld:C0031069
;
a
sio:SIO_001122
.
}
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_provenance
{
dgn-np:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_assertion
dcterms:description
"[To assess the protective as well as the modulating affect of MEFV mutation carriage on various inflammatory disease states, we sought to define the frequency of MEFV mutations in Israeli Jewish individuals of various ethnicities, including those with low frequency of FMF, which were not in the focus of our attention hitherto.]. 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:19373257
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP54773.RAXCku8VAlkLZx6AD2oYHxS9WSQFlC_dABEihIaskuwZU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}