Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion> ?p ?o ?g. }
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- NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion type Assertion NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_head.
- NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion description "[Autosomal recessive Robinow syndrome is caused by mutations in ROR2 and is characterized by short stature, mesomelic limb shortening, brachydactyly, vertebral abnormalities, and a characteristic 'fetal face' dysmorphology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_provenance.
- NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion evidence source_evidence_literature NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_provenance.
- NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion SIO_000772 15952209 NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_provenance.
- NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion wasDerivedFrom befree-20150227 NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_provenance.
- NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_assertion wasGeneratedBy ECO_0000203 NP600535.RApmVJ1J5kh6FoUfMNqnVeGqMF6s-gHhgGeBCIhnvRmmw130_provenance.