Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP790114.RALvB8pBfV2UaVb3UybPSKcxckTKe6U_kbwhNfbyhpXXQ130_provenance.