@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:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_head { this: np:hasAssertion dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_assertion; np:hasProvenance dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_provenance; np:hasPublicationInfo dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_publicationInfo; a np:Nanopublication . dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_assertion a np:Assertion . dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_provenance a np:Provenance . dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_publicationInfo a np:PublicationInfo . } dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_assertion { miriam-gene:2169 a ncit:C16612 . lld:C0271650 a ncit:C7057 . dgn-gda:DGN6d3c05a009c2fbb4063ead2593bce968 sio:SIO_000628 miriam-gene:2169, lld:C0271650; a sio:SIO_001121 . } dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_provenance { dgn-np:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_assertion dcterms:description "[(1) The Ala54 and Thr54 allele frequencies in Chinese were 0.71 and 0.29 respectively; (2) The FABP2-Ala54Thr variation was neither associated with fasting and post-challenged plasma glucose levels nor with NIDDM; (3) This variation was neither associated with fasting lipid profile nor with obesity; (4) The IGT subjects with genotype Thr54(+) (Thr54 homozygotes and heterozygotes) had lower fasting, 2-hour and total C-peptide levels and smaller AUC representing lesser C-peptide secretion after glucose challenge than those with genotype Thr54(-) (Ala54 homozygotes) (P = 0.04, 0.03, 0.01 and 0.01 respectively).]. 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:11593593; 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:NP736596.RAedVAoXqAFn8sdgK9MZx5mCYJSwhtobCQiEP64cXwt9I130_publicationInfo { this: dcterms:created "2014-10-02T12:39:27+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }