@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI
> .
@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/v4.0.0/void/
> .
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_head
{
this:
np:hasAssertion
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion
;
np:hasProvenance
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion
a
np:Assertion
.
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_provenance
a
np:Provenance
.
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN06b35187112d65ad6695366c606b911f
sio:SIO_000628
miriam-gene:3064
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_provenance
{
dgn-np:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_assertion
dcterms:description
"[As a Mendelian neurodegenerative disorder, the genetic risk of Huntington's disease (HD) is conferred entirely by an HTT CAG repeat expansion whose length is the primary determinant of the rate of pathogenesis leading to disease onset.]. 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:26232222
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1291584.RA52VqTrNQ47JBWzbNMawUbmQDtteWRVOGD5FMnPg4zkI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:31+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: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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}