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- source_evidence_literature type ECO_0000212 NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_assertion description "[Among 18 BCR-ABL+ leukemias presenting acquired trisomy of chromosome 21, we report a high frequency (33%) of recurrent point mutations (4 in myeloid blast crisis [BC] CML and one in chronic phase CML) within the DNA-binding region of RUNX1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_assertion evidence source_evidence_literature NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_assertion SIO_000772 18202228 NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_assertion wasDerivedFrom befree-20150227 NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_assertion wasGeneratedBy ECO_0000203 NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285045.RAif0-0737XP6TfdlK9AuoLjX2xRasPbumPA9w__W_1SE130_provenance.