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- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion type Assertion NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_head.
- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion wasGeneratedBy ECO_0000203 NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance.
- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion wasDerivedFrom befree-20150227 NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance.
- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion SIO_000772 11297579 NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance.
- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion evidence source_evidence_literature NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance.
- NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831504.RAsPDQDdYv46WMgH6kmzr2pDx_Zd9Kx1qJg9-nMO9ipT4130_provenance.