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- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion type Assertion NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_head.
- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion wasGeneratedBy ECO_0000203 NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_provenance.
- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion wasDerivedFrom befree-2016 NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_provenance.
- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion SIO_000772 14962902 NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_provenance.
- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion evidence source_evidence_literature NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_provenance.
- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion description "[By phenotypic analysis of affected relatives and carriers of the same ELA2 mutations, we showed that the expression of neutropenia in CN and SCN may be either homogeneous or variable according to the type of mutations, suggesting different pathogenetic mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_provenance.