Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion> ?p ?o ?g. }
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- NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion type Assertion NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_head.
- NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion wasGeneratedBy ECO_0000203 NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_provenance.
- NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion wasDerivedFrom befree-2016 NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_provenance.
- NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion SIO_000772 21533187 NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_provenance.
- NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion evidence source_evidence_literature NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_provenance.
- NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_assertion description "[MC is clinically distinct from other multiple exostosis or multiple enchondromatosis syndromes and is unlinked to EXT1 and EXT2, the genes responsible for autosomal dominant multiple osteochondromas (MO).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890803.RADWup0L1sMZsWhbScdTl2nDi4k6oq90jfuDWDTKGjkUE130_provenance.