Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_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." NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_assertion evidence source_evidence_literature NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_assertion SIO_000772 20818383 NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_assertion wasDerivedFrom befree-20140225 NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_assertion wasGeneratedBy ECO_0000203 NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP744149.RAt_3lz5rbR9W3beBqePEzdyl8fSOqfvrxYSDQyKyKriY130_provenance.