@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE
> .
@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:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_head
{
this:
np:hasAssertion
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion
;
np:hasProvenance
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion
a
np:Assertion
.
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_provenance
a
np:Provenance
.
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion
{
miriam-gene:5071
a
ncit:C16612
.
lld:C0013384
a
ncit:C7057
.
dgn-gda:DGNfd4f6cfa83fcb3bb9ad059623973141f
sio:SIO_000628
miriam-gene:5071
,
lld:C0013384
;
a
sio:SIO_001121
.
}
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_provenance
{
dgn-np:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_assertion
dcterms:description
"[None of them displayed any of the clinical hallmarks described in patients with previously reported parkin mutations, including diurnal fluctuations, benefit from sleep, foot dystonia, hyperreflexia, and early susceptibility to levodopa-induced dyskinesias.]. 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:10894217
;
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:NP875096.RAua6yavbS_N7ux5t2Q4XhEvmDXM4hTaTDQSxRKebHzTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}