@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI
> .
@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:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_head
{
this:
np:hasAssertion
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_assertion
;
np:hasProvenance
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_provenance
;
np:hasPublicationInfo
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_assertion
a
np:Assertion
.
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_provenance
a
np:Provenance
.
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_assertion
{
miriam-gene:55824
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN1d0be51f4bcbbadbcb83556a90ce708e
sio:SIO_000628
miriam-gene:55824
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_provenance
{
dgn-np:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_assertion
dcterms:description
"[Expanded polyglutamine repeats have been proposed to cause neuronal degeneration in Huntington's disease (HD) and related disorders, through abnormal interactions with other proteins containing short polyglutamine tracts such as the transcriptional coactivator CREB binding protein, CBP.]. 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:11264541
;
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:NP168997.RA4KNTZPXb80S6Q7BUU0qIe8cItL5eQBC7SxfLIRrvqqI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}