Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_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." NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_assertion evidence source_evidence_literature NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_assertion SIO_000772 20818383 NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_assertion wasDerivedFrom befree-20150227 NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_assertion wasGeneratedBy ECO_0000203 NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919199.RAfLldGRNpcpnQjgE1LCqNsWEv1ouYXk4AE8gjuWu4V18130_provenance.