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- source_evidence_literature type ECO_0000212 NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_assertion description "[Acquired molecular abnormalities (mutations or chromosomal translocations) of the RUNX1 transcription factor gene are frequent in acute myeloblastic leukemias (AMLs) and in therapy-related myelodysplastic syndromes, but rarely in acute lymphoblastic leukemias (ALLs) and chronic myelogenous leukemias (CMLs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_assertion evidence source_evidence_literature NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_assertion SIO_000772 18202228 NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_assertion wasDerivedFrom befree-20150227 NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_assertion wasGeneratedBy ECO_0000203 NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285039.RAANW89DBaEYHNiBA0tcXsaQVhwfKuIGjaUtGqOEFLTzY130_provenance.