@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc
> .
@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:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_head
{
this:
np:hasAssertion
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_assertion
;
np:hasProvenance
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_provenance
;
np:hasPublicationInfo
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_assertion
a
np:Assertion
.
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_provenance
a
np:Provenance
.
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_assertion
{
miriam-gene:2548
a
ncit:C16612
.
lld:C1135868
a
ncit:C7057
.
dgn-gda:DGNc77e831c9dcd46866d42038c270c992d
sio:SIO_000628
miriam-gene:2548
,
lld:C1135868
;
a
sio:SIO_001121
.
}
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_provenance
{
dgn-np:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_assertion
dcterms:description
"[When the size distributions of trinucleotide repeats were compared to previously reported data, significant differences were found for the CTT repeat, which corresponds to the expanded GAA repeat in Friedreich ataxia, as well as for ATT, CCT and GTT repeats.]. 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:9002673
;
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:NP521398.RAGKa0uxIq6jO2dGjqX0HVcknVgQyKvEfI3EeEQ1LJQNc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:10+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" .
}