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- source_evidence_literature type ECO_0000212 NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_assertion description "[High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_assertion evidence source_evidence_literature NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_assertion SIO_000772 14615365 NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_assertion wasDerivedFrom befree-2016 NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_assertion wasGeneratedBy ECO_0000203 NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.
- befree-2016 importedOn "2016-02-19" NP420588.RAUNdptSQVoNWIPugAEfi8SnXBWub2X8K6LQlNsPx8heo130_provenance.