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- NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_assertion type Assertion NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_head.
- NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_assertion wasGeneratedBy ECO_0000203 NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_provenance.
- NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_assertion wasDerivedFrom befree-20140225 NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_provenance.
- NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_assertion SIO_000772 12874780 NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_provenance.
- NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_assertion evidence source_evidence_literature NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_provenance.
- NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_assertion description "[AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608435.RAKlnjodzPv9_oA6HvbCMW4Juzsw61qj94fyLFdunrJ1I130_provenance.