@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_head
{
this:
np:hasAssertion
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_assertion
;
np:hasProvenance
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_provenance
;
np:hasPublicationInfo
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_assertion
a
np:Assertion
.
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_provenance
a
np:Provenance
.
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_assertion
{
miriam-gene:5428
a
ncit:C16612
.
lld:C0162670
a
ncit:C7057
.
dgn-gda:DGN7e6b190b04cf8c76d742549c16005df6
sio:SIO_000628
miriam-gene:5428
,
lld:C0162670
;
a
sio:SIO_001121
.
}
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_provenance
{
dgn-np:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_assertion
dcterms:description
"[The most recently described mitochondrial myopathies are due to defects in nuclear DNA, including coenzyme Q10 deficiency and mutations in genes controlling mitochondrial DNA abundance and structure, such as POLG, TK2, and MPV17.]. 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:17053512
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP419883.RAYZK2DCpJZqXikkedHiTysNevV7ya04RaozJq_fFqL5E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}