Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion> ?p ?o ?g. }
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- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion type Assertion NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_head.
- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion evidence source_evidence_literature NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion SIO_000772 15064611 NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion wasDerivedFrom befree-2016 NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion wasGeneratedBy ECO_0000203 NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.