Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_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." NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_assertion evidence source_evidence_curated NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_assertion SIO_000772 22057234 NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_assertion wasDerivedFrom ctd_human-2016 NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_assertion wasGeneratedBy ECO_0000218 NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_provenance.