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- NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_assertion type Assertion NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_head.
- NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_assertion description "[Mutations in several genes, including PINK1 and Parkin, are known to cause autosomal recessive cases of Parkinson disease in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_provenance.
- NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_assertion evidence source_evidence_literature NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_provenance.
- NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_assertion SIO_000772 25404737 NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_provenance.
- NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_assertion wasDerivedFrom befree-2016 NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_provenance.
- NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_assertion wasGeneratedBy ECO_0000203 NP1238128.RAMUv6QpA1sIao-U03sEoIT1_NnHgfWsI8j4P34d0ekWM130_provenance.