@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE
> .
@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:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_head
{
this:
np:hasAssertion
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_assertion
;
np:hasProvenance
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_provenance
;
np:hasPublicationInfo
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_assertion
a
np:Assertion
.
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_provenance
a
np:Provenance
.
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_assertion
{
miriam-gene:85300
a
ncit:C16612
.
lld:C0007760
a
ncit:C7057
.
dgn-gda:DGNba054c590803e951a087084b167671b0
sio:SIO_000628
miriam-gene:85300
,
lld:C0007760
;
a
sio:SIO_001121
.
}
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_provenance
{
dgn-np:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_assertion
dcterms:description
"[Mutations in Atcay/ATCAY have been identified as causative of cerebellar disorders such as the rare hereditary disease Cayman ataxia in humans, generalized dystonia in the dystonic (dt) rat, and marked motor defects in three ataxic mouse lines.]. 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:23226316
;
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:NP218347.RA54-u69kXsDbEEYKSJdTpMnTw0SqI8T7sKNlDTrk9fkE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}