Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion type Assertion NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_head.
- NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion description "[We found a high incidence of ASXL1 mutation in MF patients (20%) and a low incidence in PV (7%) and ET (4%) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_provenance.
- NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion evidence source_evidence_literature NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_provenance.
- NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion SIO_000772 22489043 NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_provenance.
- NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion wasDerivedFrom befree-20140225 NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_provenance.
- NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_assertion wasGeneratedBy ECO_0000203 NP480761.RAI7AWo2DCjb7TtBjFWVP-vxcvfqtqZAWW4rnUcJRlTro130_provenance.