@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA
> .
@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:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_assertion
a
np:Assertion
.
dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_provenance
a
np:Provenance
.
dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_assertion
{
miriam-gene:4096
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN2d7a8e866c26d8c6fc27494368394c3f
sio:SIO_000628
miriam-gene:4096
,
lld:C0525045
;
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.
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dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_provenance
{
dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_assertion
dcterms:description
"[The findings of anticipation in this study of families with UPAD and previous findings in families with BPAD suggest that the variable expression of unstable expansions of trinucleotide repeats may turn out to be the basis of the continuum of liability in affective disorders.]. 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:8557885
;
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 .
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dgn-np:NP287944.RAvMkVPaPfXsTgkirSknq13wVJTRhvHUAzEaKctFLiGVA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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
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<
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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