Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion> ?p ?o ?g. }
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- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion type Assertion NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_head.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion wasGeneratedBy ECO_0000203 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion wasDerivedFrom befree-2016 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion SIO_000772 16931578 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion evidence source_evidence_literature NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion description "[The V617F mutation is present in blood and marrow from a large proportion of patients with classic BCR/ABL-negative chronic myeloproliferative disorders and of a few patients with other clonal hematological diseases such as myelodysplastic syndrome, atypical myeloproliferative disorders, and acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.