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- source_evidence_literature type ECO_0000212 NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_assertion evidence source_evidence_literature NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_assertion SIO_000772 21266382 NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_assertion wasDerivedFrom befree-2016 NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_assertion wasGeneratedBy ECO_0000203 NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- befree-2016 importedOn "2016-02-19" NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.