@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc
> .
@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:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_head
{
this:
np:hasAssertion
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion
;
np:hasProvenance
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance
;
np:hasPublicationInfo
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion
a
np:Assertion
.
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance
a
np:Provenance
.
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion
{
miriam-gene:4287
a
ncit:C16612
.
lld:C0024408
a
ncit:C7057
.
dgn-gda:DGN0c42658c74c261bd6460b6eb15875cae
sio:SIO_000628
miriam-gene:4287
,
lld:C0024408
;
a
sio:SIO_001121
.
}
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_provenance
{
dgn-np:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_assertion
dcterms:description
"[Machado-Joseph disease (MJD), one of the most common types of hereditary spinocerebellar degeneration caused by abnormal expansion of the CAG repeat in the MJD1 gene, presents atrophy of the infratentorial structures neuropathologically and neuroradiologically.]. 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:18042234
;
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:NP167991.RACy8CnyOh-GXMgkJGY5rYGAQvBINHJxp1ElmpJcGiZBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}