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> .
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http://semanticscience.org/resource/
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@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
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http://rdf.disgenet.org/v4.0.0/void/
> .
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a
ncit:C16612
.
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a
ncit:C7057
.
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,
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dgn-np:NP118179.RAChRQdhEAWHTzAcDAE98ihkP6EuGX2VmPQWLg_eL244Y130_assertion
dcterms:description
"[In addition, SNPs in the ARNTL2, CLOCK, DBP, and TIMELESS genes and haplotypes in the ARNTL, CLOCK, CSNK1E, and TIMELESS genes showed suggestive evidence of association with several circadian phenotypes identified in BP patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:18228528
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xsd:date
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dgn-void:source_evidence_literature
a
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rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
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dgn-np:NP118179.RAChRQdhEAWHTzAcDAE98ihkP6EuGX2VmPQWLg_eL244Y130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
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