@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0
> .
@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:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_head
{
this:
np:hasAssertion
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_assertion
;
np:hasProvenance
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_assertion
a
np:Assertion
.
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_provenance
a
np:Provenance
.
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_assertion
{
miriam-gene:5521
a
ncit:C16612
.
lld:C0007758
a
ncit:C7057
.
dgn-gda:DGNf0461df9d2a602602623b3939938add8
sio:SIO_000628
miriam-gene:5521
,
lld:C0007758
;
a
sio:SIO_001121
.
}
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_provenance
{
dgn-np:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_assertion
dcterms:description
"[Spinocerebellar ataxia type 12 (SCA12) is an autosomal dominant cerebellar ataxia associated with the expansion of an unstable CAG repeat in the 5' region of the PPP2R2B gene on chromosome 5q31-5q32.]. 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:16138911
;
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:NP172455.RACVm79cfEmV1xAPVTeaA4ryxK2VyUm5vacS7JmwdQxn0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}