@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg
> .
@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:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_head
{
this:
np:hasAssertion
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_assertion
;
np:hasProvenance
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_assertion
a
np:Assertion
.
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_provenance
a
np:Provenance
.
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_assertion
{
miriam-gene:55486
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNc495794f8d54b4a51e080c9b353d2e42
sio:SIO_000628
miriam-gene:55486
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_provenance
{
dgn-np:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_assertion
dcterms:description
"[Interestingly, impaired mitophagy, an important autophagic quality control mechanism that clears the cells of damaged mitochondria, may also be an underlying mechanism of disease pathogenesis in patients for Parkinson's disease with the PARL mutations.]. 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:23533695
;
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:NP660507.RAaKqNIh95ZKIKkrfMsKL0QsJgDnrO5hw6dU2c_hgIdHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}