@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE
> .
@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:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_head
{
this:
np:hasAssertion
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_assertion
;
np:hasProvenance
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_provenance
;
np:hasPublicationInfo
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_assertion
a
np:Assertion
.
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_provenance
a
np:Provenance
.
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C3489733
a
ncit:C7057
.
dgn-gda:DGNa5c5c3f9bbc74b619f5441bc8ded6879
sio:SIO_000628
miriam-gene:2395
,
lld:C3489733
;
a
sio:SIO_001121
.
}
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_provenance
{
dgn-np:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_assertion
dcterms:description
"[Machado-Joseph disease (spinocerebellar ataxia type 3) (prevalence, 3.1 per 100,000 population), Friedreich ataxia (prevalence, 1.0 per 100,000 population), and ataxia with oculomotor apraxia (prevalence, 0.4 per 100,000 population) were the most frequent HCAs.]. 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:23609960
;
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:NP722865.RAQSd5Egi07yf0R20tR9vcR_tInV7ttrWS48KjAZ3l1OE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}