Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion> ?p ?o ?g. }
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- NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion type Assertion NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_head.
- NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion description "[Autosomal recessive Robinow syndrome is caused by mutations in ROR2 and is characterized by short stature, mesomelic limb shortening, brachydactyly, vertebral abnormalities, and a characteristic `fetal face` dysmorphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_provenance.
- NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion evidence source_evidence_literature NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_provenance.
- NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion SIO_000772 15952209 NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_provenance.
- NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion wasDerivedFrom befree-20140225 NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_provenance.
- NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_assertion wasGeneratedBy ECO_0000203 NP389276.RAo8mHgDWK4ZxoPMBRWo6REGJITdbXAsBJqJXAR9nMMho130_provenance.