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- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion type Assertion NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_head.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion wasGeneratedBy ECO_0000203 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion wasDerivedFrom lhgdn-20090331 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion SIO_000772 18536571 NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion evidence source_evidence_literature NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.
- NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_assertion description "[REVIEW: Congenital neutropenia patients with acquired CSF3R mutations define a group with high risk for development of leukemia; discussion of possible pathomechanism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238597.RARpj_4o33ZXgYnDD_CdRA8VqPxll3-379-nDku3Mt6HQ130_provenance.