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- NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_assertion type Assertion NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_head.
- NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_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." NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_provenance.
- NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_assertion evidence source_evidence_literature NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_provenance.
- NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_assertion SIO_000772 17665217 NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_provenance.
- NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_assertion wasDerivedFrom befree-2016 NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_provenance.
- NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_assertion wasGeneratedBy ECO_0000203 NP622594.RAQdV0hPr2pmBNjdVNCTQ58bRQjdViTfqJVamFAwLunC8130_provenance.