@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc
> .
@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:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_head
{
this:
np:hasAssertion
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_assertion
;
np:hasProvenance
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_provenance
;
np:hasPublicationInfo
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_assertion
a
np:Assertion
.
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_provenance
a
np:Provenance
.
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_assertion
{
miriam-gene:56652
a
ncit:C16612
.
lld:C0271385
a
ncit:C7057
.
dgn-gda:DGN977f6b01abc28d2bb6234f4c2611f2ae
sio:SIO_000628
miriam-gene:56652
,
lld:C0271385
;
a
sio:SIO_001121
.
}
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_provenance
{
dgn-np:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_assertion
dcterms:description
"[The six identified SCA8 patients were clinically characterized by high frequencies of incoordination of trunk and limbs, ataxic dysarthria, impaired smooth pursuit, and horizontal nystagmus, and the MRI showed significant atrophy of the cerebellar vermis and hemispheres compared with that of normal controls.]. 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:10690991
;
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:NP820814.RArKlf82U4A0J2S3IzO0oP9bm8yi-L4-gQ23q_cfoeRBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}