Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion> ?p ?o ?g. }
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- NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion type Assertion NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_head.
- NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion description "[While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_provenance.
- NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion evidence source_evidence_literature NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_provenance.
- NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion SIO_000772 19507262 NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_provenance.
- NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion wasDerivedFrom befree-20140225 NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_provenance.
- NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_assertion wasGeneratedBy ECO_0000203 NP534553.RAqUsHGa2SLkYh6bDVHsVVWr4rNvsvIRaTtuKWpGLT4yk130_provenance.