Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion description "[Intriguingly, mutations in an NMD factor, Upf3b, have been found in patients with autism [2, 3].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion evidence source_evidence_literature NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion SIO_000772 23638902 NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion wasDerivedFrom befree-2016 NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion wasGeneratedBy ECO_0000203 NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_provenance.