Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion> ?p ?o ?g. }
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- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion type Assertion NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_head.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_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." NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion evidence source_evidence_literature NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion SIO_000772 15952209 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion wasDerivedFrom befree-20140225 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.
- NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_assertion wasGeneratedBy ECO_0000203 NP315586.RANmptkkHgOq5acRLPccWsk83juQsz7uFbAFes1ZwscsY130_provenance.