Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion> ?p ?o ?g. }
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- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion type Assertion NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_head.
- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion description "[Using exome sequencing of individuals with Myhre syndrome, we identified SMAD4 as a candidate gene that contributes to this syndrome on the basis of its pivotal role in the bone morphogenetic pathway (BMP) and transforming growth factor (TGF)- signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_provenance.
- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion evidence source_evidence_curated NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_provenance.
- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion SIO_000772 22158539 NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_provenance.
- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion wasDerivedFrom ctd_human-20130708 NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_provenance.
- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion wasGeneratedBy ECO_0000218 NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_provenance.