@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:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_head { this: np:hasAssertion dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion; np:hasProvenance dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_provenance; np:hasPublicationInfo dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_publicationInfo; a np:Nanopublication . dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion a np:Assertion . dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_provenance a np:Provenance . dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_publicationInfo a np:PublicationInfo . } dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion { miriam-gene:2572 a ncit:C16612 . lld:C0028756 a ncit:C7057 . dgn-gda:DGN324d29302ba03bb3ce0da35dcb0f2201 sio:SIO_000628 miriam-gene:2572, lld:C0028756; a sio:SIO_001121 . } dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_provenance { dgn-np:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_assertion dcterms:description "[Potential confounding variables in association studies involving common variants and complex diseases (low power to detect modest genetic effects, overinterpretation of marginal data, population stratification, and biological plausibility) are also discussed in the context of GAD2 and severe obesity.]. 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:16122350; 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:NP510562.RAsoVbYiAVATtYwjX8SP-ArIdmFJu4n2IIhvfd5WFeBCM130_publicationInfo { this: dcterms:created "2016-05-13T12:45:36+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" . }