Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP629372.RAwYWdrcSwkNMjC0ZDazl1r8GGURvHx6wl2yg0w8BbBIs130_provenance.