Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion> ?p ?o ?g. }
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- NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_assertion type Assertion NP587.RA3cjNMyCX4r0SAL19R4dWrggCyhN_e9RXdOus0czH-wA130_head.
- 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.