Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion type Assertion NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_head.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion wasGeneratedBy ECO_0000203 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion wasDerivedFrom befree-20140225 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion SIO_000772 19473076 NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_assertion evidence source_evidence_literature NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.
- NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_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." NP860113.RAaoqaQvJBJhMojH9jlMde1BwEkwq9Z2Iq2IdUE8uaHns130_provenance.