@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_assertion
a
np:Assertion
.
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_provenance
a
np:Provenance
.
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:56652
a
ncit:C16612
.
lld:C0751651
a
ncit:C7057
.
dgn-gda:DGNddd252aa5adca7da5620067c04a8e6e3
sio:SIO_000628
miriam-gene:56652
,
lld:C0751651
;
a
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.
}
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_provenance
{
dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_assertion
dcterms:description
"[This review focuses on our current knowledge of genetic defects of mtDNA replication (POLG, POLG2, C10orf2) and nucleotide metabolism (TYMP, TK2, DGOUK, and RRM2B) that cause instability of mtDNA and mitochondrial disease.]. 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:22176657
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP923891.RA54ilQiG4pKj7oJerS_XhZoXWMWSwVVw1XCYt75bAwgM130_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
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;
pav:authoredBy
<
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> , <
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> , <
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" .
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pav:version
"v3.0.0" .
}