Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion> ?p ?o ?g. }
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- NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion type Assertion NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_head.
- NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion wasGeneratedBy ECO_0000203 NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_provenance.
- NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion wasDerivedFrom befree-20140225 NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_provenance.
- NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion SIO_000772 23018678 NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_provenance.
- NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion evidence source_evidence_literature NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_provenance.
- NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_assertion description "[Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536088.RAH1sCpa834g98lvhH_9pXmufKsdn-qQ986FqdoDI8kac130_provenance.