Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_assertion description "[Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_assertion evidence source_evidence_literature NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_assertion SIO_000772 22057234 NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_assertion wasDerivedFrom befree-2016 NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_assertion wasGeneratedBy ECO_0000203 NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP936554.RAD4Y-nHOjjIZqf4orotOLXE9zjcUzVLxa5nQWOt0JKkQ130_provenance.