@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI
> .
@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:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_head
{
this:
np:hasAssertion
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion
;
np:hasProvenance
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_provenance
;
np:hasPublicationInfo
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion
a
np:Assertion
.
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_provenance
a
np:Provenance
.
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGN706a697d87a9bbd41f08327eccf3831e
sio:SIO_000628
miriam-gene:4210
,
lld:C0031069
;
a
sio:SIO_001122
.
}
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_provenance
{
dgn-np:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_assertion
dcterms:description
"[A total of 19 FMF patients and eight healthy individuals were genotyped for mutations in the MEFV gene and gut bacterial diversity was assessed by sequencing 16S rRNA gene libraries and FISH analysis.]. 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:18725973
;
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:NP54776.RAjsNtkup_-odWGQE0EnVjhxw0AlW4ySMM67Bn3N5YZtI130_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" .
}