@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI
> .
@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:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_head
{
this:
np:hasAssertion
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_assertion
;
np:hasProvenance
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_provenance
;
np:hasPublicationInfo
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_assertion
a
np:Assertion
.
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_provenance
a
np:Provenance
.
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0087012
a
ncit:C7057
.
dgn-gda:DGN892e74280cafd1934a4203f9010d281c
sio:SIO_000628
miriam-gene:367
,
lld:C0087012
;
a
sio:SIO_001121
.
}
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_provenance
{
dgn-np:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_assertion
dcterms:description
"[The disease is one of nine inherited neurodegenerative disorders that are caused by this type of mutation, and which include dentatorubral pallidoluysian atrophy, spinal and bulbar muscular atrophy, and the spinocerebellar ataxias 1, 2, 3, 6, 7, and 17.]. 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:12747895
;
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:NP738371.RAKDhIr9Vao-bVGHO4_UbD-jZ3y88-t9CXNc_WbMIT4PI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:28+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" .
}