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- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_assertion type Assertion NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_head.
- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_assertion wasGeneratedBy ECO_0000203 NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_provenance.
- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_assertion wasDerivedFrom befree-20150227 NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_provenance.
- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_assertion SIO_000772 16385458 NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_provenance.
- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_assertion evidence source_evidence_literature NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_provenance.
- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_assertion description "[Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_provenance.