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- NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_assertion type Assertion NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_head.
- NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_assertion description "[Deficiency of the paternal 15q11-q13 snoRNA HBII-85 locus is necessary to cause the neurodevelopmental disorder Prader-Willi syndrome (PWS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_provenance.
- NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_assertion evidence source_evidence_literature NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_provenance.
- NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_assertion SIO_000772 19656775 NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_provenance.
- NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_assertion wasDerivedFrom befree-20150227 NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_provenance.
- NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_assertion wasGeneratedBy ECO_0000203 NP959237.RAxtEFT6WuJ7wzshq8JmfPlvsHeoqhtBs0HaJBZkyu-A8130_provenance.