Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_assertion> ?p ?o ?g. }
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- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_assertion type Assertion NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_head.
- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_assertion wasGeneratedBy ECO_0000203 NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_provenance.
- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_assertion wasDerivedFrom lhgdn-20090331 NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_provenance.
- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_assertion SIO_000772 16385458 NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_provenance.
- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_assertion evidence source_evidence_literature NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_provenance.
- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_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." NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_provenance.