@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY
> .
@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:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_head
{
this:
np:hasAssertion
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion
;
np:hasProvenance
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_provenance
;
np:hasPublicationInfo
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion
a
np:Assertion
.
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_provenance
a
np:Provenance
.
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0087012
a
ncit:C7057
.
dgn-gda:DGN125a609714ba7330397b964483d416a7
sio:SIO_000628
miriam-gene:3064
,
lld:C0087012
;
a
sio:SIO_001121
.
}
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_provenance
{
dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion
dcterms:description
"[The two shorter constructs containing the beta A4 sequence formed similar intranuclear aggregates to those reported for intranuclear inclusions of polyglutamine peptides from huntingtin (in Huntington's disease) and ataxin protein fragments (in spinocerebellar 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:9686302
;
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:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:31+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: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" .
}