Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_assertion> ?p ?o ?g. }
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- NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_assertion type Assertion NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_head.
- NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_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." NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_provenance.
- NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_assertion evidence source_evidence_curated NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_provenance.
- NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_assertion SIO_000772 22057234 NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_provenance.
- NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_assertion wasDerivedFrom ctd_human-20150221 NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_provenance.
- NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_assertion wasGeneratedBy ECO_0000218 NP18101.RAoNFCEspuQ0A4P_QcX0bNK_rDvFXFgfEKw-TDXICDT4I130_provenance.