Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_assertion> ?p ?o ?g. }
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- NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_assertion type Assertion NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_head.
- NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_assertion wasGeneratedBy ECO_0000218 NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_provenance.
- NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_assertion wasDerivedFrom uniprot-2016 NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_provenance.
- NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_assertion SIO_000772 12414817 NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_provenance.
- NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_assertion evidence source_evidence_curated NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_provenance.
- NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_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." NP2359.RAp78jKSEJwgQPGSSemK5e7SyGUKS2n_z0qrwhCoDk1cc130_provenance.