@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:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_head { this: np:hasAssertion dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion; np:hasProvenance dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance; np:hasPublicationInfo dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_publicationInfo; a np:Nanopublication . dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion a np:Assertion . dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance a np:Provenance . dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_publicationInfo a np:PublicationInfo . } dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion { miriam-gene:3630 a ncit:C16612 . lld:C0011849 a ncit:C7057 . dgn-gda:DGN38e1f02c8fa171aaae99be1661c4a1ce sio:SIO_000628 miriam-gene:3630, lld:C0011849; a sio:SIO_001121 . } dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance { dgn-np:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion dcterms:description "[Until recently, HI was generally considered an orphan disease, but as parallel defects in ion channels, enzymes, and metabolic pathways also give rise to diabetes and impaired insulin release, the HI paradigm has wider implications for more common disorders of the endocrine pancreas and the molecular physiology of ion transport.]. 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:14715916; 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:NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_publicationInfo { this: dcterms:created "2016-05-13T12:44:59+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" . }