Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion> ?p ?o ?g. }
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- NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_assertion type Assertion NP1074475.RActbRNsnnoshrJGVku5DdP_AvFtWQUZO_L1y2eV9G1KQ130_head.
- 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.