Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_assertion description "[Significantly, these abnormalities are similar to the skeletal anomalies found in trisomy-16 mice and in humans with Down's syndrome, wherein the dosage of Ets2 is known to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_assertion evidence source_evidence_literature NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_assertion SIO_000772 11175361 NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_assertion wasDerivedFrom befree-2016 NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_assertion wasGeneratedBy ECO_0000203 NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.
- befree-2016 importedOn "2016-02-19" NP307130.RATlPSriShhO-e_1kKkYDyxJH5tG9qsCOJ1mhDZyU9VhA130_provenance.