@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4
> .
@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/v3.0.0/void/
> .
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_head
{
this:
np:hasAssertion
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_assertion
;
np:hasProvenance
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_assertion
a
np:Assertion
.
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_provenance
a
np:Provenance
.
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_assertion
{
miriam-gene:6311
a
ncit:C16612
.
lld:C0004134
a
ncit:C7057
.
dgn-gda:DGN24d4b556b7d771302d7e99e8c74dc744
sio:SIO_000628
miriam-gene:6311
,
lld:C0004134
;
a
sio:SIO_001121
.
}
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_provenance
{
dgn-np:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_assertion
dcterms:description
"[Preclinical SCA1 and SCA2 mutation carriers seem to have mild coordination deficits and abnormalities in the brain that are more common in carriers who are closer to the estimated onset of ataxia.]. 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:23707147
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP681666.RAwMeg8xVoogMeL66gh4BvxCNAEXlx4Ca3oufTAv7OlL4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:31+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}