Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion> ?p ?o ?g. }
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- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion type Assertion NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_head.
- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_provenance.
- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion evidence source_evidence_literature NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_provenance.
- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion SIO_000772 17665217 NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_provenance.
- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion wasDerivedFrom befree-20150227 NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_provenance.
- NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_assertion wasGeneratedBy ECO_0000203 NP674263.RA0Ez0b3ugAq9xVuAlaC-Tsrq9w4hGlHYzwDM6r2o5W6A130_provenance.