Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_assertion description "[Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_assertion evidence source_evidence_curated NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_assertion SIO_000772 14614622 NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_assertion wasDerivedFrom uniprot-2016 NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_assertion wasGeneratedBy ECO_0000218 NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3091.RAJCZSULmjcb57Xlp-Ti3M6huNUI5-Osq52XUINA2u8Pk130_provenance.