@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:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_head { this: np:hasAssertion dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_assertion; np:hasProvenance dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_provenance; np:hasPublicationInfo dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_publicationInfo; a np:Nanopublication . dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_assertion a np:Assertion . dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_provenance a np:Provenance . dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_publicationInfo a np:PublicationInfo . } dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_assertion { miriam-gene:5092 a ncit:C16612 . lld:C0342276 a ncit:C7057 . dgn-gda:DGN8fdc1bb3e349b31a1e8f8a77ac867640 sio:SIO_000628 miriam-gene:5092, lld:C0342276; a sio:SIO_001121 . } dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_provenance { dgn-np:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_assertion dcterms:description "[Overall, our findings establish PCBD1 as a coactivator of the HNF1B-mediated transcription necessary for fine tuning FXYD2 transcription in the DCT and suggest that patients with HPABH4D should be monitored for previously unrecognized late complications, such as hypomagnesemia and MODY diabetes.]. 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:24204001; 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:NP1126009.RAkxCOVdBAWf3aXcSFZq3BPptJxYiFdFHuxRAG-3Zn96g130_publicationInfo { this: dcterms:created "2016-05-13T12:50:16+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" . }