@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU
> .
@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:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_head
{
this:
np:hasAssertion
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion
;
np:hasProvenance
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_provenance
;
np:hasPublicationInfo
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion
a
np:Assertion
.
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_provenance
a
np:Provenance
.
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion
{
miriam-gene:4287
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGN4e04fb0afabe3ed30988c2286f8de9b1
sio:SIO_000628
miriam-gene:4287
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_provenance
{
dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion
dcterms:description
"[Clinical dysfunction as measured by the Scale for the Assessment and Rating of Ataxia (SARA) and the Unified Huntington's Disease Rating Scale functional assessment correlated best with the atrophy of pons in SCA1, with total brainstem atrophy in SCA3 and atrophy of total cerebellum in SCA6.]. 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:19631275
;
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:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}