Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion> ?p ?o ?g. }
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- NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion type Assertion NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_head.
- NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion description "[Focusing on cytogenetic aberrations most commonly found in MDS, we retrospectively genotyped 566 MDS/AML patients carrying -5/del(5q), -7/del(7q), +8, del(20q) and -Y.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_provenance.
- NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion evidence source_evidence_literature NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_provenance.
- NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion SIO_000772 23643325 NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_provenance.
- NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion wasDerivedFrom befree-20150227 NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_provenance.
- NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_assertion wasGeneratedBy ECO_0000203 NP873099.RAohIcIuyyazbEti8tLt-4C1vP5FPniZRDtcL1BeZ2txw130_provenance.