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- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion type Assertion NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_head.
- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion description "[Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_provenance.
- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion evidence source_evidence_curated NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_provenance.
- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion SIO_000772 23857908 NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_provenance.
- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion wasDerivedFrom uniprot-2016 NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_provenance.
- NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_assertion wasGeneratedBy ECO_0000218 NP7589.RAR99CRP-mk2-zvtRfEvPbLq6KHMVjIbuXq3ONqKmbijg130_provenance.