Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_assertion> ?p ?o ?g. }
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- NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_assertion type Assertion NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_head.
- NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_assertion wasGeneratedBy ECO_0000203 NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_provenance.
- NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_assertion wasDerivedFrom befree-20150227 NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_provenance.
- NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_assertion SIO_000772 21533187 NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_provenance.
- NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_assertion evidence source_evidence_literature NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_provenance.
- NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_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." NP388402.RAGN38vv2AHPgxU2tZSmCRkwiDevq_7y6xsgQcG1KQCZc130_provenance.