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- NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_assertion type Assertion NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_head.
- NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_assertion description "[Mutations in ROR2, encoding the receptor tyrosine kinase-like orphan receptor 2, cause two distinct skeletal diseases: autosomal dominant brachydactyly type B1 (BDB1) and autosomal recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_provenance.
- NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_assertion evidence source_evidence_literature NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_provenance.
- NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_assertion SIO_000772 19461659 NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_provenance.
- NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_assertion wasDerivedFrom befree-2016 NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_provenance.
- NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_assertion wasGeneratedBy ECO_0000203 NP740530.RABXhgjnDwicWO7rspeSkEnlmqglfz69jl_PN_Dywnyzo130_provenance.