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- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion type Assertion NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_head.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion description "[Somatic, heterozygous ASXL1 mutations were identified in 14/48 (29%) of patients with GATA2 deficiency, including four out of five patients who developed a proliferative chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion evidence source_evidence_literature NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion SIO_000772 24077845 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion wasDerivedFrom befree-2016 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.
- NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_assertion wasGeneratedBy ECO_0000203 NP1114756.RAunaPgDq7B9gKE_e5SaHYloM6NDaceFinSixIdki8eMw130_provenance.