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- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion type Assertion NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_head.
- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_provenance.
- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion evidence source_evidence_literature NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_provenance.
- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion SIO_000772 20400963 NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_provenance.
- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion wasDerivedFrom befree-2016 NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_provenance.
- NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_assertion wasGeneratedBy ECO_0000203 NP806790.RAr-TMxgRS4hO89G7n53xdV83Co8-fiTbhuDStyqtaWL8130_provenance.