Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion> ?p ?o ?g. }
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- NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion type Assertion NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_head.
- NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion description "[The cytogenetic anomaly der(20)del(20)(q11.2q13.3)idic(20)(p11), or idic(20q-) in short form, has been reported in 13 cases of myelodysplastic syndrome, one case of chronic myelomonocytic leukemia, and one case of acute myeloid leukemia since 2004.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_provenance.
- NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion evidence source_evidence_literature NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_provenance.
- NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion SIO_000772 18262055 NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_provenance.
- NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion wasDerivedFrom befree-20140225 NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_provenance.
- NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_assertion wasGeneratedBy ECO_0000203 NP181483.RAgIlojdVZ6tIfi4VOUAhae1qxqLD0TE0MOv7GgOxUUd0130_provenance.