@prefix bfo: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix dcterms: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_head {
this: np:hasAssertion dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_assertion;
np:hasProvenance dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_provenance;
np:hasPublicationInfo dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_publicationInfo;
a np:Nanopublication .
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_assertion a np:Assertion .
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_provenance a np:Provenance .
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_publicationInfo a
np:PublicationInfo .
}
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_assertion {
miriam-gene:9314 a ncit:C16612 .
lld:C0011860 a ncit:C7057 .
dgn-gda:DGNf945365b864c94f94deb4ebea1275bfa sio:SIO_000628 miriam-gene:9314, lld:C0011860;
a sio:SIO_001121 .
}
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_provenance {
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_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-2016;
prov:wasGeneratedBy bfo:ECO_0000203 .
dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
dgn-void:source_evidence_literature a bfo:ECO_0000212;
rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP624270.RAFVF-gOA5iMog44HvTcRLE2mGyoN5EbyqngFanfxY_xs130_publicationInfo {
this: dcterms:created "2016-05-13T12:46:28+02:00"^^xsd:dateTime;
dcterms:rights ;
dcterms:rightsHolder dgn-void:IBIGroup;
dcterms:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy , ,
, , ;
pav:createdBy ;
pav:version "v4.0.0.0" .
dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}