Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion> ?p ?o ?g. }
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- NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion type Assertion NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_head.
- NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion wasGeneratedBy ECO_0000203 NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_provenance.
- NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion wasDerivedFrom befree-20150227 NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_provenance.
- NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion SIO_000772 21326312 NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_provenance.
- NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion evidence source_evidence_literature NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_provenance.
- NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_assertion description "[Our finding suggests that hypospadias associated with hypertelorism is the mildest phenotype in OS caused by MID1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556427.RA9T0SBYFyNbCMD4iokGBsACquuLKg5cW70LvEJMhQWio130_provenance.