Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_assertion> ?p ?o ?g. }
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- NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_assertion type Assertion NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_head.
- NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_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." NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_assertion evidence source_evidence_literature NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_assertion SIO_000772 17846414 NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_assertion wasDerivedFrom befree-2016 NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_assertion wasGeneratedBy ECO_0000203 NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.