Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_assertion type Assertion NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_head.
- NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_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." NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_provenance.
- NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_assertion evidence source_evidence_literature NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_provenance.
- NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_assertion SIO_000772 21350094 NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_provenance.
- NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_assertion wasDerivedFrom befree-20150227 NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_provenance.
- NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_assertion wasGeneratedBy ECO_0000203 NP978662.RAROEw9Nc-Yv26kZmmOTBx9ao5HV2NZC2g5pFm7mXunws130_provenance.