@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg
> .
@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:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_head
{
this:
np:hasAssertion
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_assertion
;
np:hasProvenance
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_provenance
;
np:hasPublicationInfo
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_assertion
a
np:Assertion
.
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_provenance
a
np:Provenance
.
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C0162670
a
ncit:C7057
.
dgn-gda:DGN6ff486c38abc55a94ee87cd6b8684221
sio:SIO_000628
miriam-gene:5428
,
lld:C0162670
;
a
sio:SIO_001121
.
}
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_provenance
{
dgn-np:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_assertion
dcterms:description
"[Most recently described mitochondrial myopathies are due to defects in nuclear DNA, including coenzyme Q10 deficiency, and mutations in genes that control mitochondrial DNA (mtDNA) abundance and structure such as POLG and TK2.]. 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:16155436
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP512962.RATgLU9w-5KFBv97fvjOSZhloCwLRq7M_W99QMoJVtfBg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:37+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" .
}