@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_head
{
this:
np:hasAssertion
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_assertion
;
np:hasProvenance
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_assertion
a
np:Assertion
.
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_provenance
a
np:Provenance
.
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0008489
a
ncit:C7057
.
dgn-gda:DGNecbc3758bc1117795b000a48ddb1811e
sio:SIO_000628
miriam-gene:3064
,
lld:C0008489
;
a
sio:SIO_001121
.
}
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_provenance
{
dgn-np:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_assertion
dcterms:description
"[Huntington's disease (HD) is a neurodegenerative genetic disorder caused by an expansion of CAG repeats in the HD gene encoding for huntingtin (Htt), resulting in progressive death of striatal neurons, with clinical symptoms of chorea, dementia and dramatic weight loss.]. 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:22150069
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP445306.RA9S1kLQoYJnH4KESdQmfJcQK5eQj-Uuq2tltujVSjCZ0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:00+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}