Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion> ?p ?o ?g. }
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- NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion type Assertion NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_head.
- NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion description "[Recently, the 5q- syndrome, a subtype of myelodysplastic syndrome characterized by a defect in erythroid differentiation, is caused by a somatically acquired deletion of chromosome 5q, which results in haploinsufficiency of RPS14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_provenance.
- NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion evidence source_evidence_literature NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_provenance.
- NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion SIO_000772 20882441 NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_provenance.
- NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion wasDerivedFrom befree-20140225 NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_provenance.
- NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_assertion wasGeneratedBy ECO_0000203 NP692220.RAOOCPIcCdlz6IeP-3E2P8GxGlba7hiMKfE54o8HYF6MA130_provenance.