@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U
> .
@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:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_head
{
this:
np:hasAssertion
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_assertion
;
np:hasProvenance
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_provenance
;
np:hasPublicationInfo
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_assertion
a
np:Assertion
.
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_provenance
a
np:Provenance
.
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_assertion
{
miriam-gene:6532
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN59543e5ec14a1237fb67e3e932e58da8
sio:SIO_000628
miriam-gene:6532
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_provenance
{
dgn-np:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_assertion
dcterms:description
"[Unintended weight loss, sleep and circadian disturbances and autonomic dysfunction are prevalent features of Huntington's disease (HD), an autosomal dominantly inherited neurodegenerative disorder caused by an expanded CAG repeat sequence in the HTT gene.]. 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:25074766
;
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:NP1206223.RAaF-pmauNQpD-kImWBE1RSqOdjjwQ8TR3e29-Zs7XL2U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:52+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" .
}