@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo
> .
@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/v3.0.0/void/
> .
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_head
{
this:
np:hasAssertion
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_assertion
;
np:hasProvenance
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_provenance
;
np:hasPublicationInfo
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_assertion
a
np:Assertion
.
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_provenance
a
np:Provenance
.
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_assertion
{
miriam-gene:9968
a
ncit:C16612
.
lld:C0162292
a
ncit:C7057
.
dgn-gda:DGNad358fbb0e574236c6294cb0095f3354
sio:SIO_000628
miriam-gene:9968
,
lld:C0162292
;
a
sio:SIO_001121
.
}
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_provenance
{
dgn-np:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_assertion
dcterms:description
"[Although OPA1 is a nuclear gene, the gene product localizes to mitochondria, suggesting that mitochondrial dysfunction may be the final common pathway for many forms of syndromic and nonsyndromic optic atrophy, hearing loss, and external ophthalmoplegia.]. 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:15531309
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP833535.RAudBmj1rTNPScTcyWM79byIf0qZtXJl74RfIgw0sHWzo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:06+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}