Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_assertion description "[Acquired mutations in GATA1 were detected in the vast majority of patients with acute megakaryoblastic leukemia (DS-AMKL) and in nearly every patient with transient myeloproliferative disorder (TMD), a `preleukemia` that may be present in as many as 10% of infants with DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_assertion evidence source_evidence_literature NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_assertion SIO_000772 14512321 NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_assertion wasDerivedFrom befree-20140225 NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_assertion wasGeneratedBy ECO_0000203 NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP683528.RAd-bBSpoM_nLyj6_XDGPiaw_x5jAuib65zvo0a-RAyLI130_provenance.