@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8
> .
@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:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_head
{
this:
np:hasAssertion
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_assertion
;
np:hasProvenance
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_provenance
;
np:hasPublicationInfo
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_assertion
a
np:Assertion
.
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_provenance
a
np:Provenance
.
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0087012
a
ncit:C7057
.
dgn-gda:DGNc7e3664401dde80ed3b36cfb56e75152
sio:SIO_000628
miriam-gene:367
,
lld:C0087012
;
a
sio:SIO_001121
.
}
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_provenance
{
dgn-np:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_assertion
dcterms:description
"[The present review highlights the importance of repeat expansions in some neuropsychiatric diseases, such as spinal and bulbular atrophy (SBMA), spinocerebellar ataxia (SCA), Huntington's disease (HD), schizophrenia, myotonic dystrophy (DM) and fragile-X syndrome.]. 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:12960939
;
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:NP931497.RAgB41SqQgL3QlM0eDoEMcMp1k0aKVELy_Wp3gkNtbCg8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}