Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion> ?p ?o ?g. }
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- NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion type Assertion NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_head.
- NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion description "[These results allow further delineation of the spectrum of malformations ascribed to SMADIP1 haploinsufficiency, which includes frequent features such as hypospadias and agenesis of the corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_provenance.
- NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion evidence source_evidence_literature NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_provenance.
- NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion SIO_000772 11595972 NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_provenance.
- NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion wasDerivedFrom befree-20140225 NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_provenance.
- NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_assertion wasGeneratedBy ECO_0000203 NP416042.RA0wzt-DsVMqytxNmi6i1AjmCXfnvriIr8GkKxW8uiOI0130_provenance.