@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A
> .
@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:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_head
{
this:
np:hasAssertion
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion
;
np:hasProvenance
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_provenance
;
np:hasPublicationInfo
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion
a
np:Assertion
.
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_provenance
a
np:Provenance
.
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGNc438a1fdedbb08b6dc473d54f38289cc
sio:SIO_000628
miriam-gene:3064
,
lld:C0020179
;
a
sio:SIO_001122
.
}
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_provenance
{
dgn-np:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_assertion
dcterms:description
"[Use of RNA interference to reduce huntingtin protein (htt) expression in affected brain regions may provide an effective treatment for Huntington disease (HD), but it remains uncertain whether suppression of both wild-type and mutant alleles in a heterozygous patient will provide more benefit than harm.]. 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:19289118
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP42625.RAJdcJvlbVzwyCyrumr1P4A3SYHlCmPFh0EyAyxJn1b9A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:19+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" .
}