Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion type Assertion NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_head.
- NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion description "[Here we report the identification of two novel mutations in the frizzled-like cysteine-rich domain of ROR2 causing Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_provenance.
- NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion evidence source_evidence_literature NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_provenance.
- NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion SIO_000772 17665217 NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_provenance.
- NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion wasDerivedFrom befree-20140225 NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_provenance.
- NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_assertion wasGeneratedBy ECO_0000203 NP717793.RApMH6guXXDhgHhv6padKvo5u1KKfs8crAzuWpSjgLF68130_provenance.