Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion> ?p ?o ?g. }
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- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion type Assertion NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_head.
- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion description "[Furthermore, an increased awareness of clinicians has helped detect a number of additional families affected by inherited myelodysplastic syndromes, resulting in the identification of novel causative mechanisms of disease, such as RUNX1 deficiency resulting from constitutional microdeletions of 21q22 and myelodysplasia-associated with telomerase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_provenance.
- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion evidence source_evidence_literature NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_provenance.
- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion SIO_000772 21606161 NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_provenance.
- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion wasDerivedFrom befree-2016 NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_provenance.
- NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_assertion wasGeneratedBy ECO_0000203 NP896265.RAgSdJY0G4Y60y0-tgD8mlbxyHH1BrtCcGamYaZ_CMf4g130_provenance.