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- NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_assertion type Assertion NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_head.
- NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_assertion wasGeneratedBy ECO_0000203 NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_provenance.
- NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_assertion wasDerivedFrom befree-2016 NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_provenance.
- NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_assertion SIO_000772 12107438 NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_provenance.
- NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_assertion evidence source_evidence_literature NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_provenance.
- NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_assertion description "[Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360091.RA5YQhKvZLSoyr_Tchwk8jDbw3RMn6Y8UngLf0zhkB_IA130_provenance.