Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_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." NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_assertion evidence source_evidence_literature NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_assertion SIO_000772 22057234 NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_assertion wasDerivedFrom befree-20140225 NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_assertion wasGeneratedBy ECO_0000203 NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP788335.RAzt2I1Ya0SreCpKIJo6uIJjM6rGW9OtGwkpvG1zb7M1E130_provenance.