@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A
> .
@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:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_head
{
this:
np:hasAssertion
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_assertion
;
np:hasProvenance
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_provenance
;
np:hasPublicationInfo
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_assertion
a
np:Assertion
.
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_provenance
a
np:Provenance
.
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_assertion
{
miriam-gene:5521
a
ncit:C16612
.
lld:C0234376
a
ncit:C7057
.
dgn-gda:DGN175c00aaeba3602074a8a629a8352daf
sio:SIO_000628
miriam-gene:5521
,
lld:C0234376
;
a
sio:SIO_001121
.
}
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_provenance
{
dgn-np:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_assertion
dcterms:description
"[SCA-12 is a slowly progressive, autosomal dominant, neurodegenerative disorder that differs from other SCA in that it typically presents with action tremor in patients in their mid 30s and usually includes hyperreflexia and subtle parkinsonian signs.]. 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:11171892
;
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:NP373809.RAV4yrlcrLvz3kEydQo190X1eQY897ejyzho3bn6if73A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}