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- NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_assertion type Assertion NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_head.
- NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_assertion description "[The classical Lesch-Nyhan syndrome has the deficiency of hypoxanthine-guanine phosphoribosyltransferase (HGPRT) activity as the result of mutation in the structural gene for the enzyme located on the X chromosome and is believed to be of X-linked recessive or sex-linked mode of inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_provenance.
- NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_assertion evidence source_evidence_literature NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_provenance.
- NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_assertion SIO_000772 7112549 NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_provenance.
- NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_assertion wasDerivedFrom befree-2016 NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_provenance.
- NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_assertion wasGeneratedBy ECO_0000203 NP1307666.RAJ7mVljbhlz3YNjun277BipELGWDRof8pgxiNFqqTX5k130_provenance.