Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_assertion type Assertion NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_head.
- NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_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." NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_provenance.
- NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_assertion evidence source_evidence_literature NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_provenance.
- NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_assertion SIO_000772 22057234 NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_provenance.
- NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_assertion wasDerivedFrom befree-20140225 NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_provenance.
- NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_assertion wasGeneratedBy ECO_0000203 NP822195.RAp1xl6YYcj_W-Bbri0N46XgGwjpEoZeSWcjyHPETdqfk130_provenance.