Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion type Assertion NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_head.
- NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion description "[RUNX1 gene alterations are associated with acquired and inherited hematologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or secondary acute myeloid leukemia, and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_provenance.
- NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion evidence source_evidence_literature NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_provenance.
- NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion SIO_000772 22677128 NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_provenance.
- NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion wasDerivedFrom befree-20140225 NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_provenance.
- NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_assertion wasGeneratedBy ECO_0000203 NP186120.RA-cJeDb-lClUA76j75KfP41uncZCO3ezDs1mcHpFS5dU130_provenance.