Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_assertion type Assertion NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_head.
- NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_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." NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_provenance.
- NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_assertion evidence source_evidence_literature NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_provenance.
- NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_assertion SIO_000772 20882441 NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_provenance.
- NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_assertion wasDerivedFrom befree-20140225 NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_provenance.
- NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_assertion wasGeneratedBy ECO_0000203 NP508622.RA8JMpoa_2Bdnb-uR3xWDGcBeURmBowkuG7AXtgpkRcAk130_provenance.