Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion> ?p ?o ?g. }
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- NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion type Assertion NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_head.
- NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion description "[We have reported dominant and recessive inheritance of parkinsonism, mitochondrial myopathy, and premature amenorrhea in five ethnically distinct families with POLG1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion evidence source_evidence_literature NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion SIO_000772 17846414 NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion wasDerivedFrom befree-20140225 NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_assertion wasGeneratedBy ECO_0000203 NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.