Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_assertion> ?p ?o ?g. }
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- NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_assertion type Assertion NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_head.
- NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_assertion wasGeneratedBy ECO_0000203 NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_provenance.
- NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_assertion wasDerivedFrom befree-20140225 NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_provenance.
- NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_assertion SIO_000772 21533187 NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_provenance.
- NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_assertion evidence source_evidence_literature NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_provenance.
- NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_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." NP643453.RAcGb3QMkmV7bLWFOTDM__Y5bsGkoHhbrzR00kZeM_5VI130_provenance.