Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion> ?p ?o ?g. }
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- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion type Assertion NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_head.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion description "[To extend these results we searched for mutations of ASXL1 in a series of chronic myelomonocytic leukaemias, a disease classified as MDS/Myeloproliferative disorder, and found mutations in 17 out of 39 patients (43%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion evidence source_evidence_literature NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion SIO_000772 19388938 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion wasDerivedFrom befree-20150227 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.
- NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_assertion wasGeneratedBy ECO_0000203 NP978462.RAf1uCj9AOj8IUBoXw4vOnhHbEL4sQz6iuZ3lX6j5PhVw130_provenance.