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- source_evidence_literature type ECO_0000212 NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.