@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM
> .
@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:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_head
{
this:
np:hasAssertion
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion
;
np:hasProvenance
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_provenance
;
np:hasPublicationInfo
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion
a
np:Assertion
.
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_provenance
a
np:Provenance
.
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion
{
miriam-gene:4566
a
ncit:C16612
.
lld:C0162671
a
ncit:C7057
.
dgn-gda:DGN685bb6c650ba4d9627eebbfc81c17a0e
sio:SIO_000628
miriam-gene:4566
,
lld:C0162671
;
a
sio:SIO_001121
.
}
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_provenance
{
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion
dcterms:description
"[Since modification of these taurine-containing uridines has been found to be lacking in mutant mitochondrial tRNAs for Leu(UUR) and Lys from pathogenic cells of the mitochondrial encephalomyopathies MELAS and MERRF, respectively, our findings will considerably deepen our understanding of the molecular pathogenesis of mitochondrial encephalomyopathic 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:12456664
;
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:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}