Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_assertion> ?p ?o ?g. }
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- NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_assertion type Assertion NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_head.
- NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_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." NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_provenance.
- NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_assertion evidence source_evidence_curated NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_provenance.
- NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_assertion SIO_000772 22057234 NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_provenance.
- NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_assertion wasDerivedFrom ctd_human-20130708 NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_provenance.
- NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_assertion wasGeneratedBy ECO_0000218 NP18892.RA4nv7X18sGHAKp-JyZzLzf-5I8c5KrKMXT-W2TN_ZltU130_provenance.