@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc
> .
@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:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_head
{
this:
np:hasAssertion
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_assertion
;
np:hasProvenance
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_provenance
;
np:hasPublicationInfo
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_assertion
a
np:Assertion
.
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_provenance
a
np:Provenance
.
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C0037773
a
ncit:C7057
.
dgn-gda:DGN2a3970da22b58bdbed5efdc22cc482b7
sio:SIO_000628
miriam-gene:2395
,
lld:C0037773
;
a
sio:SIO_001121
.
}
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_provenance
{
dgn-np:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_assertion
dcterms:description
"[Moreover, mitochondrial dysfunction plays an important role in the pathophysiology of several well established nuclear genetic disorders, such as dominant optic atrophy (mutations in OPA1), Friedreich's ataxia (FRDA), hereditary spastic paraplegia (SPG7), and Wilson's disease (ATP7B).]. 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:12933917
;
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:NP558733.RACcDy0Nf92IjPJd1e4mD7fYSEcEJjaCtkudVCR1PFNCc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}