Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_assertion description "[High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_assertion evidence source_evidence_literature NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_assertion SIO_000772 20818383 NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_assertion wasDerivedFrom befree-2016 NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_assertion wasGeneratedBy ECO_0000203 NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.
- befree-2016 importedOn "2016-02-19" NP837321.RAFuNboep7z7rCfDl-1LtuGKhsO5esNH-L_P--K6q9gb0130_provenance.