Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_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." NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_assertion evidence source_evidence_literature NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_assertion SIO_000772 14615365 NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_assertion wasDerivedFrom befree-2016 NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_assertion wasGeneratedBy ECO_0000203 NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.
- befree-2016 importedOn "2016-02-19" NP420587.RAqoxI5pOZI7tyzCMa7lpT_Fskis9CsjukWp7SQPXM31M130_provenance.