@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY
> .
@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/v3.0.0/void/
> .
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_head
{
this:
np:hasAssertion
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_assertion
;
np:hasProvenance
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_assertion
a
np:Assertion
.
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_provenance
a
np:Provenance
.
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_assertion
{
miriam-gene:56652
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNeefbdd6e3c51d6c805db4e00d76dd955
sio:SIO_000628
miriam-gene:56652
,
lld:C0026986
;
a
sio:SIO_001122
.
}
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_provenance
{
dgn-np:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_assertion
dcterms:description
"[MDS are due to defects in mtDNA maintenance caused by mutations in nuclear genes that function in either mitochondrial nucleotide synthesis (TK2, SUCLA2, SUCLG1, RRM2B, DGUOK, and TYMP) or mtDNA replication (POLG and C10orf2).]. 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:23385875
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP923807.RAL1ULG4rNhjENbZR6eKBB4vDCDWhRWC5705OLIUvzJUY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:04+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}