Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_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." NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_assertion evidence source_evidence_literature NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_assertion SIO_000772 14615365 NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_assertion wasDerivedFrom befree-20140225 NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_assertion wasGeneratedBy ECO_0000203 NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217765.RAJQKPQvbR5WaFe4vEd5e5Oaqaa9514t-sD8ecZ3xQcNI130_provenance.