@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc
> .
@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/v4.0.0/void/
> .
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_head
{
this:
np:hasAssertion
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_assertion
;
np:hasProvenance
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_assertion
a
np:Assertion
.
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_provenance
a
np:Provenance
.
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_assertion
{
miriam-gene:5071
a
ncit:C16612
.
lld:C0598589
a
ncit:C7057
.
dgn-gda:DGNcd6b0a9e8c0e40c90893c698a3966ce1
sio:SIO_000628
miriam-gene:5071
,
lld:C0598589
;
a
sio:SIO_001121
.
}
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_provenance
{
dgn-np:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_assertion
dcterms:description
"[Mutations causing genetic forms of Parkinson's disease or hereditary neuropathies have been recently shown to affect key molecular players involved in the recycling of defective mitochondria, most notably PARKIN, PINK1, Mitofusin 2 or dynein heavy chain.]. 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:23958438
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1103598.RAIcZ7-z2o0kK5rUc77LXtkDFQ19qeiYX8fymFpbArQEc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:06+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}