@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ
> .
@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:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_head
{
this:
np:hasAssertion
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_assertion
;
np:hasProvenance
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_assertion
a
np:Assertion
.
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_provenance
a
np:Provenance
.
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_assertion
{
miriam-gene:5339
a
ncit:C16612
.
lld:C0008489
a
ncit:C7057
.
dgn-gda:DGN2daefcbfd4ef1287f3c4968b06accfb7
sio:SIO_000628
miriam-gene:5339
,
lld:C0008489
;
a
sio:SIO_001121
.
}
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_provenance
{
dgn-np:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_assertion
dcterms:description
"[A transgenic primate model for Huntington's Disease (HD) first reported by our group that (HD monkeys) carry the mutant Huntingtin (HTT) gene with expanded polyglutamine (CAG) repeats and, develop chorea, dystonia, and other involuntary motor deficiencies similar to HD [ 1 ].]. 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:23190281
;
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:NP485538.RA3VEoquxIItOo-rs_vEchs-DY1nHAmHHbdme4536RtUQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}