Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion wasGeneratedBy ECO_0000218 NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion wasDerivedFrom uniprot-20130724 NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion SIO_000772 12414817 NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion evidence source_evidence_curated NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion description "[Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_provenance.