Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_assertion description "[Resequencing of 13 uveal melanomas with partial monosomy 3 identified 8 tumors with a mutation in either SF3B1 (7; 54%) or EIF1AX (1; 8%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_assertion evidence source_evidence_literature NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_assertion SIO_000772 23793026 NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_assertion wasDerivedFrom befree-2016 NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_assertion wasGeneratedBy ECO_0000203 NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1088233.RAccvuTW1jWOJHS0vwA59tq2H2I32WTURylqKJVg6QcwQ130_provenance.