Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_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." NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_assertion evidence source_evidence_curated NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_assertion SIO_000772 22057234 NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_assertion wasDerivedFrom ctd_human-20130708 NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_assertion wasGeneratedBy ECO_0000218 NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP18890.RAXCxQLzhzKT2BuVjGfiYEPXYrWYiNZAALx59y88ZmgI8130_provenance.