@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic
> .
@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:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_head
{
this:
np:hasAssertion
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_assertion
;
np:hasProvenance
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_provenance
;
np:hasPublicationInfo
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_assertion
a
np:Assertion
.
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_provenance
a
np:Provenance
.
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_assertion
{
miriam-gene:6310
a
ncit:C16612
.
lld:C1839259
a
ncit:C7057
.
dgn-gda:DGN1e285b91254361678abc0f44b10bff03
sio:SIO_000628
miriam-gene:6310
,
lld:C1839259
;
a
sio:SIO_001121
.
}
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_provenance
{
dgn-np:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_assertion
dcterms:description
"[A feature of these diseases is ubiquitinated intraneuronal inclusions derived from the mutant proteins, which colocalize with heat shock proteins (HSPs) in SCA1 and SBMA and proteasomal components in SCA1, SCA3, and SBMA.]. 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:10717003
;
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:NP677371.RAtq6IdiDfKgkWYZhssqGXOvY59LAO7TN4nnbXEOmc_Ic130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}