Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion> ?p ?o ?g. }
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- NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion type Assertion NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_head.
- NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion description "[Among the cell strains that did not show RDS were two from AT obligate heterozygotes (i.e., the parents of AT patients), two from patients with Alzheimer disease, two from patients with Friedreich ataxia, one from a patient with Bloom syndrome, one from a patient with Down syndrome, and six from patients with various immunodeficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_provenance.
- NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion evidence source_evidence_literature NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_provenance.
- NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion SIO_000772 2722185 NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_provenance.
- NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion wasDerivedFrom befree-2016 NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_provenance.
- NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_assertion wasGeneratedBy ECO_0000203 NP1296344.RAGQ30uhRPCoNzrYAaN11yV5-3RxSBLczX93ZHolH3BvI130_provenance.