@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U
> .
@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:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_head
{
this:
np:hasAssertion
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_assertion
;
np:hasProvenance
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_provenance
;
np:hasPublicationInfo
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_assertion
a
np:Assertion
.
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_provenance
a
np:Provenance
.
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_assertion
{
miriam-gene:688
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN6e9146bddc86ea57d4555129d18d417c
sio:SIO_000628
miriam-gene:688
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_provenance
{
dgn-np:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_assertion
dcterms:description
"[These SNPs, located in the KLF2, KLF4 and KLF5 gene were then analysed in our second replication set, but analysis of this set and the combined analysis of the three variants in all 2,219 individuals did not show an association with T2D in this French population.]. 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:17688680
;
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:NP484819.RA_t_U5atqssWuCIbnhG6cP-Zj5rr7sMcqQxQyBCBOa5U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}