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- NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_assertion type Assertion NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_head.
- NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_assertion wasGeneratedBy ECO_0000203 NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_provenance.
- NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_assertion wasDerivedFrom befree-20150227 NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_provenance.
- NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_assertion SIO_000772 19473076 NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_provenance.
- NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_assertion evidence source_evidence_literature NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_provenance.
- NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_assertion description "[Congenital contractural arachnodactyly (Beals syndrome) is a rare autosomal dominantly inherited connective tissue disorder characterized by flexion contractures, arachnodactyly, crumpled ears, and mild muscular hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396062.RABHc3OOxo82lhM5aey2vDtM0vvDCc1_oWxgJxTeQKvfA130_provenance.