Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion> ?p ?o ?g. }
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- NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion type Assertion NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_head.
- NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion description "[Here we demonstrate that runx1 deletion in mice induces the persistence of MYH10 in platelets, and a similar persistence was observed in platelets of patients with constitutional (familial platelet disorder/acute myeloid leukemia) or acquired (chronic myelomonocytic leukemia) RUNX1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_provenance.
- NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion evidence source_evidence_literature NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_provenance.
- NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion SIO_000772 22677128 NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_provenance.
- NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion wasDerivedFrom befree-20150227 NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_provenance.
- NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_assertion wasGeneratedBy ECO_0000203 NP583698.RAlNXLxJAC0FWzLHAWonoAsc-WK8ZUlr1mGqZEWsMqpoI130_provenance.