@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o
> .
@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:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_head
{
this:
np:hasAssertion
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_assertion
;
np:hasProvenance
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_assertion
a
np:Assertion
.
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_provenance
a
np:Provenance
.
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_assertion
{
miriam-gene:7084
a
ncit:C16612
.
lld:C0162670
a
ncit:C7057
.
dgn-gda:DGN8d74de2104b22d8dc241fd768b8468fd
sio:SIO_000628
miriam-gene:7084
,
lld:C0162670
;
a
sio:SIO_001121
.
}
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_provenance
{
dgn-np:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_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-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:NP626925.RA3ft2g1MisJlKlCJE1aukmJf7yRhZIUu4V6kG2rZOv0o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}