Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion> ?p ?o ?g. }
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- NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion type Assertion NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_head.
- NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion description "[The chromosomal abnormality der(17)t(12;17)(q13;p13) is very rare in hematologic malignancies, and has been reported in only two patients with therapy-related acute myeloid leukemia (t-AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_provenance.
- NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion evidence source_evidence_literature NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_provenance.
- NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion SIO_000772 19155067 NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_provenance.
- NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion wasDerivedFrom befree-2016 NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_provenance.
- NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_assertion wasGeneratedBy ECO_0000203 NP715438.RAU1aCxe4sq0mVW9FXWIKRDqSM-EKSPH5ZtTp7PFjSdGk130_provenance.