@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs
> .
@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:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_head
{
this:
np:hasAssertion
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_assertion
;
np:hasProvenance
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_assertion
a
np:Assertion
.
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_provenance
a
np:Provenance
.
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_assertion
{
miriam-gene:1890
a
ncit:C16612
.
lld:C0477402
a
ncit:C7057
.
dgn-gda:DGN05213895f348dd8c6e0a153dc7aa0ca9
sio:SIO_000628
miriam-gene:1890
,
lld:C0477402
;
a
sio:SIO_001121
.
}
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_provenance
{
dgn-np:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_assertion
dcterms:description
"[This study stresses the insidious heterogeneous clinical onset of some cases of MNGIE, expands the spectrum of the phenotype, and suggests considering MNGIE in the differential diagnosis of enteropathic arthritis, isolated exercise intolerance, and inflammatory polyneuropathies not responsive to the usual treatment.]. 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:21503690
;
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:NP716546.RA3rgvJ2h-GSJR7Vp0wx-VuC35uDLpRCF4-y95vvTMZYs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}