Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion> ?p ?o ?g. }
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- NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion type Assertion NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_head.
- NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion description "[The remaining cases usually lack the JAK2(V617F)mutation, have a platelet count less than 600 � 10(3)/?L (600 � 10(9)/L), and may represent an MDS or MPN with thrombocytosis of unknown mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_provenance.
- NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion evidence source_evidence_literature NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_provenance.
- NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion SIO_000772 21350094 NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_provenance.
- NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion wasDerivedFrom befree-20150227 NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_provenance.
- NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_assertion wasGeneratedBy ECO_0000203 NP781567.RAk95F1vO731RVDS7VVMoBBVpTFKVufnQ7NnPs647WrCM130_provenance.