Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion> ?p ?o ?g. }
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- NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion type Assertion NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_head.
- NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion description "[A systematic RNA interference screen to interrogate the function of each gene in the common deleted region (CDR) for the 5q- syndrome identified RPS14 as a critical haploinsufficiency disease gene for the erythroid failure, which is a characteristic of this syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_provenance.
- NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion evidence source_evidence_literature NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_provenance.
- NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion SIO_000772 19322210 NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_provenance.
- NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion wasDerivedFrom befree-2016 NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_provenance.
- NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_assertion wasGeneratedBy ECO_0000203 NP728562.RAn9VNx6WkR0gY7C6aUSCAs7SBywv4R5CtxvOpul5Z6mI130_provenance.