@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:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_head { this: np:hasAssertion dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_assertion; np:hasProvenance dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_provenance; np:hasPublicationInfo dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_publicationInfo; a np:Nanopublication . dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_assertion a np:Assertion . dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_provenance a np:Provenance . dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_publicationInfo a np:PublicationInfo . } dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_assertion { miriam-gene:1184 a ncit:C16612 . lld:C0020438 a ncit:C7057 . dgn-gda:DGN00f82817ea81c3b305a6948f6341b35b sio:SIO_000628 miriam-gene:1184, lld:C0020438; a sio:SIO_001121 . } dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_provenance { dgn-np:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_assertion dcterms:description "[Dent's disease, an X-linked disorder characterized by low molecular weight proteinuria, hypercalciuria, and nephrolithiasis, is due to mutations of the chloride/proton antiporter, CLC-5; ADHH is associated with activating mutations of the calcium-sensing receptor, which is a G protein-coupled receptor; hypophosphatemic hypercalciuric nephrolithiasis associated with rickets is due to mutations in the type 2c sodium-phosphate cotransporter (NPT2c); and familial hypomagnesemia with hypercalciuria is due to mutations of paracellin-1, which is a member of the claudin family of membrane proteins that form the intercellular tight junction barrier in a variety of epithelia.]. 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:17872384; 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:NP630221.RAB9cj1OE51RrFdChVyiZvG31xIfCGPSrFQfHsitZljjA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:31+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" . }