Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion> ?p ?o ?g. }
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- NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion type Assertion NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_head.
- NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion description "[Future studies to define the mechanism that results in the high frequency of GATA1 mutations in DS and the role of altered GATA1 in TMD and DS-AMKL will shed light on the multistep pathway in human leukemia and may lead to an increased understanding of why children with DS are markedly predisposed to leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_provenance.
- NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion evidence source_evidence_literature NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_provenance.
- NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion SIO_000772 14512321 NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_provenance.
- NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion wasDerivedFrom befree-2016 NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_provenance.
- NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_assertion wasGeneratedBy ECO_0000203 NP414769.RAb63XM51hses1GYxw2xMI51ZMNFzg9DBZNHsc1mnshtQ130_provenance.