Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion type Assertion NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_head.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion wasGeneratedBy ECO_0000218 NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_provenance.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion wasDerivedFrom uniprot-20130724 NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_provenance.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion SIO_000772 16385458 NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_provenance.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion evidence source_evidence_curated NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_provenance.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_assertion description "[Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_provenance.