@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_assertion
;
np:hasProvenance
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_provenance
;
np:hasPublicationInfo
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_assertion
a
np:Assertion
.
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_provenance
a
np:Provenance
.
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_assertion
{
miriam-gene:9030
a
ncit:C16612
.
lld:C1970945
a
ncit:C7057
.
dgn-gda:DGN303ce5e4dd50ae4ba8661b9fb6cdcc63
sio:SIO_000628
miriam-gene:9030
,
lld:C1970945
;
a
sio:SIO_001121
.
}
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_provenance
{
dgn-np:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_assertion
dcterms:description
"[The purpose of the present study was to further test if expanded CAG repeats detected by the repeat expansion detection (RED) method in bipolar affective disorder (BPAD) are correlated with ERDA1 (17q21.3) and/or CTG18.1 (18q21.1) loci expansions, and changes of phenotype severity in successive generations (anticipation).]. 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:15211635
;
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:NP769577.RAnHeNRDciv3Vrmm5JzLvTQimsdr9sxnvylTP7nWgR14s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}