@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E
> .
@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:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_head
{
this:
np:hasAssertion
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion
;
np:hasProvenance
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_provenance
;
np:hasPublicationInfo
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion
a
np:Assertion
.
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_provenance
a
np:Provenance
.
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C1843920
a
ncit:C7057
.
dgn-gda:DGNef49c61b9722848411be7283b43122e9
sio:SIO_000628
miriam-gene:5428
,
lld:C1843920
;
a
sio:SIO_001121
.
}
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_provenance
{
dgn-np:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_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:NP512961.RAfN6bi3c5zDfkLADPqiHcko-ALGw3BhC36hhzYI_1U0E130_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" .
}