@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o
> .
@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:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_head
{
this:
np:hasAssertion
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_assertion
;
np:hasProvenance
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_provenance
;
np:hasPublicationInfo
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_assertion
a
np:Assertion
.
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_provenance
a
np:Provenance
.
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_assertion
{
miriam-gene:6310
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN26854badbf6ebd7f9e4ba007f48aa38c
sio:SIO_000628
miriam-gene:6310
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_provenance
{
dgn-np:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_assertion
dcterms:description
"[Genetic analysis performed on a large Thai kindred with autosomal dominant cerebellar ataxia, in which frontal lobe signs and dementia are commonly observed in affected family members, exclude linkage to the SCA1, SCA2 and MJD loci.]. 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:8162021
;
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:NP778060.RAhi714XzK1zcqf3PCCujFHlqA2ZShfc5y8MhRQcJyy3o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}