@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:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_head { this: np:hasAssertion dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_assertion; np:hasProvenance dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_provenance; np:hasPublicationInfo dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_publicationInfo; a np:Nanopublication . dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_assertion a np:Assertion . dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_provenance a np:Provenance . dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_publicationInfo a np:PublicationInfo . } dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_assertion { miriam-gene:3991 a ncit:C16612 . lld:C0920563 a ncit:C7057 . dgn-gda:DGNd39181343f394099a7e21f322f3ff3c5 sio:SIO_000628 miriam-gene:3991, lld:C0920563; a sio:SIO_001122 . } dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_provenance { dgn-np:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_assertion dcterms:description "[We conclude that a number of genetic polymorphisms in HSL exist, some of which are highly prevalent. Neither of the polymorphisms we identified in the coding region, however, contributed measurably to the biological variation of insulin sensitivity in ou]. 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:11714847; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP69708.RAkVkEFAlt8xrbuY0GQqLscCHoAiph3aj487TqfqXM9B4130_publicationInfo { this: dcterms:created "2015-08-25T14:38:18+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }