Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion type Assertion NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_head.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion wasGeneratedBy ECO_0000218 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion wasDerivedFrom uniprot-20130724 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion SIO_000772 10925378 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion evidence source_evidence_curated NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.