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- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion type Assertion NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_head.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion wasGeneratedBy ECO_0000203 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion wasDerivedFrom befree-2016 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion SIO_000772 20830319 NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion evidence source_evidence_literature NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.
- NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838331.RAh3F8rmjPsSiJ2FLg6MbO1MYawBjRFwVB1HStxf0Cax8130_provenance.