Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion> ?p ?o ?g. }
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- NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion type Assertion NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_head.
- NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion wasGeneratedBy ECO_0000203 NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_provenance.
- NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion wasDerivedFrom befree-20140225 NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_provenance.
- NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion SIO_000772 8913726 NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_provenance.
- NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion evidence source_evidence_literature NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_provenance.
- NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_assertion description "[The review of eight similar, previously reported cases and the clinical, cytogenetic, and molecular studies performed in our patients led us to make the following observations: (I) CT8M predisposes to neoplasms, preferentially to myelo- or lymphoproliferative diseases; (2) a gene dosage effect for glutathione reductase in red blood cells was seen in two of our patients; (3) the wide phenotypic variation of CT8M was confirmed: trisomy 8 in neoplastic cells of phenotypically near-normal cases may be misinterpreted as acquired; and (4) molecular studies suggested a postzygotic origin of the trisomy in our three cases, with the supernumerary chromosome being of paternal origin in one case and of maternal origin in the other two.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686037.RAi9WBaKvo-ozyDNPKE4OmXyKScvXBDiV0WS3sel1mNuE130_provenance.