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- NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_assertion type Assertion NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_head.
- NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_assertion description "[These results suggest that homozygous mutations in SLC26A4 are always associated with EVA, while the severity of cochlear malformation may vary depending on the type of SLC26A4 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_provenance.
- NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_assertion evidence source_evidence_literature NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_provenance.
- NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_assertion SIO_000772 25468468 NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_provenance.
- NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_assertion wasDerivedFrom befree-2016 NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_provenance.
- NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_assertion wasGeneratedBy ECO_0000203 NP1244271.RALMCgnJbNWy8ibnT7TxWsnMSZW0BPeEUyldkx9HVvztc130_provenance.