@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU
> .
@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
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;
np:hasProvenance
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dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_assertion
a
np:Assertion
.
dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_provenance
a
np:Provenance
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dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_publicationInfo
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}
dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_assertion
{
miriam-gene:1797
a
ncit:C16612
.
lld:C0795864
a
ncit:C7057
.
dgn-gda:DGNa04a951b232ccf276bb264745640089b
sio:SIO_000628
miriam-gene:1797
,
lld:C0795864
;
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.
}
dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_provenance
{
dgn-np:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_assertion
dcterms:description
"[Data further show that haploinsufficiency of RAI1 and Rai1 in SMS fibroblasts and the mouse hypothalamus, respectively, results in the transcriptional dysregulation of the circadian clock and causes altered expression and regulation of multiple circadian genes, including PER2, PER3, CRY1, BMAL1, and others.]. 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:22578325
;
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:NP266010.RAuHTIi-JwNYOpVm4X21E4xqPcelq9EWrO6FF1lj3HsEU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+02:00"^^
xsd:dateTime
;
dcterms:rights
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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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pav:authoredBy
<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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pav:version
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