Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually 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.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion evidence source_evidence_curated NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion SIO_000772 10925378 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion wasDerivedFrom uniprot-20130724 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_assertion wasGeneratedBy ECO_0000218 NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3486.RAZtaY8tBSJnIw3V3g59e9VvMQ_yucIpmYo_TlmXWXTbs130_provenance.