Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion> ?p ?o ?g. }
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- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion type Assertion NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_head.
- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_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." NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_provenance.
- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion evidence source_evidence_literature NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_provenance.
- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion SIO_000772 21606161 NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_provenance.
- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion wasDerivedFrom befree-20140225 NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_provenance.
- NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_assertion wasGeneratedBy ECO_0000203 NP718032.RAsuzXADrjefshWe35hdDiKk4tzFLibGjHNtOJZT0ZgIg130_provenance.