@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y
> .
@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:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_head
{
this:
np:hasAssertion
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_assertion
;
np:hasProvenance
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_assertion
a
np:Assertion
.
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_provenance
a
np:Provenance
.
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGN2057c907541c2b1c9550775c646244be
sio:SIO_000628
miriam-gene:3064
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_provenance
{
dgn-np:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_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-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:NP367012.RAs15us8OvHy3YBmOzDB3hZlkzc6V6DIa-ZlAhtHf8T4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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" .
}