@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A
> .
@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#
> .
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_head
{
this:
np:hasAssertion
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_assertion
;
np:hasProvenance
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_provenance
;
np:hasPublicationInfo
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_assertion
a
np:Assertion
.
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_provenance
a
np:Provenance
.
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_assertion
{
miriam-gene:79068
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGN510afc78a7e5883f7f99b322d709b865
sio:SIO_000628
miriam-gene:79068
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_provenance
{
dgn-np:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_assertion
dcterms:description
"[The aim of this study was to clarify the role of single nucleotide polymorphisms (SNPs) in FTO in metabolic disorders such as hypertension, obesity, diabetes, dyslipidemia, insulin resistance and metabolic syndrome in the Japanese general population using data from a cohort study in Hokkaido, namely the Tanno-Sobetsu study.]. 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:20075932
;
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:NP643218.RADiCs-nEcwm4QdDRkcy6XIejyhGKpEWM_YqRzFBACR5A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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" .
}