@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE
> .
@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:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_assertion
;
np:hasProvenance
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_provenance
;
np:hasPublicationInfo
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_assertion
a
np:Assertion
.
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_provenance
a
np:Provenance
.
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_assertion
{
miriam-gene:4544
a
ncit:C16612
.
lld:C0037317
a
ncit:C7057
.
dgn-gda:DGNd7e86d8b2dfdbb4ddf686c2949dfc6ee
sio:SIO_000628
miriam-gene:4544
,
lld:C0037317
;
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.
}
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_provenance
{
dgn-np:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_assertion
dcterms:description
"[The aim of this study was to investigate whether the MTNR1B gene variant rs10830963 is associated with sleep problems and whether this variant contributes to the association between sleep disturbances and type 2 diabetes.]. 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:21380592
;
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:NP762046.RA2pTT104lWfkhej8NaxBmi8ypGmP4yxkiOpoxA4ZO8eE130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v2.1.0" .
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