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- NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_assertion type Assertion NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_head.
- NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_assertion wasGeneratedBy ECO_0000218 NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_provenance.
- NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_assertion wasDerivedFrom uniprot-2016 NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_provenance.
- NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_assertion SIO_000772 15001591 NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_provenance.
- NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_assertion evidence source_evidence_curated NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_provenance.
- NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_assertion description "[Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3299.RAfPPP4p97KSWCi4o8hHPGuylGwUPC00FT5PtBKPM_cuE130_provenance.