Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_assertion> ?p ?o ?g. }
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- NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_assertion type Assertion NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_head.
- NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_assertion wasGeneratedBy ECO_0000203 NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_provenance.
- NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_assertion wasDerivedFrom befree-20140225 NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_provenance.
- NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_assertion SIO_000772 19473076 NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_provenance.
- NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_assertion evidence source_evidence_literature NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_provenance.
- NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_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." NP338686.RAvAfQHf5ffNTwQof7jGqTPo9DRI66LQgj9TuK5LKoONg130_provenance.