@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ
> .
@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:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_head
{
this:
np:hasAssertion
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_assertion
;
np:hasProvenance
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_assertion
a
np:Assertion
.
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_provenance
a
np:Provenance
.
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_assertion
{
miriam-gene:1371
a
ncit:C16612
.
lld:C0268237
a
ncit:C7057
.
dgn-gda:DGNb46523a063f5d8e30f90917eeef9caa8
sio:SIO_000628
miriam-gene:1371
,
lld:C0268237
;
a
sio:SIO_001121
.
}
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_provenance
{
dgn-np:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_assertion
dcterms:description
"[Consequently, cytochrome oxidase (COX) deficiency was found in all these (LS(COX)) cell lines and, thus, the main mitochondrial mechanism of generation of the electrochemical proton gradient on the mitochondrial membrane was naturally depressed.]. 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:11341780
;
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:NP160137.RA_BMfG3tE9Z82WFFIl93DTsyiH5J4JLnMSAA91YLb2HQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}