Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_assertion description "[Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_assertion evidence source_evidence_curated NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_assertion SIO_000772 22019273 NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_assertion wasDerivedFrom uniprot-2016 NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_assertion wasGeneratedBy ECO_0000218 NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6826.RAHguP5hxNIkQwyqPd4Q2NvywBoaJ4sRYdntEHeU_dI9A130_provenance.