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- NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_assertion type Assertion NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_head.
- NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_assertion description "[In summary, it is unlikely that the typical Young syndrome patient has a clinical disease associated with CFTR mutation on both alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_provenance.
- NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_assertion evidence source_evidence_literature NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_provenance.
- NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_assertion SIO_000772 7551394 NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_provenance.
- NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_assertion wasDerivedFrom befree-20140225 NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_provenance.
- NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_assertion wasGeneratedBy ECO_0000203 NP462869.RATEYWhe5D0issoFTmh8iomdY7X2UjL2roYVxt_9BU1gU130_provenance.