@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_head { this: np:hasAssertion dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_assertion; np:hasProvenance dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_provenance; np:hasPublicationInfo dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_publicationInfo; a np:Nanopublication . dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_assertion a np:Assertion . dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_provenance a np:Provenance . dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_publicationInfo a np:PublicationInfo . } dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_assertion { miriam-gene:2696 a ncit:C16612 . lld:C0011860 a ncit:C7057 . dgn-gda:DGNdba1f40653b9604153c6cb0ed5b36cf6 sio:SIO_000628 miriam-gene:2696, lld:C0011860; a sio:SIO_001121 . } dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_provenance { dgn-np:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_assertion dcterms:description "[We found no detectable effect (with an OR >2.1) of the variants in GCKR, GIPR, ADCY5 and VPS13C on the response to sulfonylurea treatment, indicating that these variants are not significantly contributing to the risk of SH in patients with T2D.]. 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:22956255; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1010963.RAhYJY_q3xdFzGnxUKhPgcrGdsIrN1nSi2uMgEhcN1CBg130_publicationInfo { this: dcterms:created "2016-05-13T12:49:24+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" . }