Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_assertion description "[in a kindred with a syndrome including hypertension, hypercholesterolemia & hypomagnesemia, analysis of maternal lineage mitochondrial genome identified a mutation substituting cytidine for uridine immediately 5'to the mitochondrial TRNA (Ile) anticodon]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_assertion evidence source_evidence_literature NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_assertion SIO_000772 15498972 NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_assertion wasDerivedFrom lhgdn-20090331 NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_assertion wasGeneratedBy ECO_0000203 NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198654.RA1G01HvPGnsRUTzWOO1RFyOXT2W_tbbad4Ey6ogK6A0c130_provenance.