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- NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_assertion type Assertion NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_head.
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- NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_assertion wasDerivedFrom uniprot-20150221 NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_provenance.
- NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_assertion SIO_000772 15001591 NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_provenance.
- NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_assertion evidence source_evidence_curated NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_provenance.
- NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_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." NP1998.RAAvw-TB8oDc9HwRN1HcW9ELLYNWnhjEmPTKNPoowBuYo130_provenance.