Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_assertion> ?p ?o ?g. }
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- NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_assertion type Assertion NP30323.RAle24w3K_B-Lia6DsU4w7ipj7VMcVa8Wj1ObFGIKK8H8130_head.
- 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.