@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_head
{
this:
np:hasAssertion
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_assertion
;
np:hasProvenance
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_assertion
a
np:Assertion
.
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_provenance
a
np:Provenance
.
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_assertion
{
miriam-gene:4553
a
ncit:C16612
.
lld:C0162671
a
ncit:C7057
.
dgn-gda:DGNbf0817064a66bfdf0945b1a0f3924d78
sio:SIO_000628
miriam-gene:4553
,
lld:C0162671
;
a
sio:SIO_001122
.
}
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_provenance
{
dgn-np:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_assertion
dcterms:description
"[Acquisition of the wobble modification in another isoacceptor tRNA is critical for suppressing the MELAS mutation, highlighting the primary role of the UUG decoding deficiency in the molecular pathogenesis of MELAS syndrome.]. 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:16446307
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:24+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}