@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM
> .
@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:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_head
{
this:
np:hasAssertion
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_assertion
;
np:hasProvenance
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_provenance
;
np:hasPublicationInfo
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_assertion
a
np:Assertion
.
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_provenance
a
np:Provenance
.
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_assertion
{
miriam-gene:7083
a
ncit:C16612
.
lld:C0162670
a
ncit:C7057
.
dgn-gda:DGN75b418e8ee4a1b51a6565c5b2062f45f
sio:SIO_000628
miriam-gene:7083
,
lld:C0162670
;
a
sio:SIO_001121
.
}
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_provenance
{
dgn-np:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_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:NP937603.RAsVnoBUTugyAhNX8cKvRlvsaV1I2Bcm3ErmasTrQnTTM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}