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- NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_assertion type Assertion NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_head.
- NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_assertion wasGeneratedBy ECO_0000203 NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_provenance.
- NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_assertion wasDerivedFrom befree-2016 NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_provenance.
- NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_assertion SIO_000772 12930917 NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_provenance.
- NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_assertion evidence source_evidence_literature NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_provenance.
- NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_assertion description "[Severe phenotype of phosphorylase kinase-deficient liver glycogenosis with mutations in the PHKG2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406260.RA3FHy_758Wryq1XBi1O9FHfIfVh3EWw6x6H3aAl89l_U130_provenance.