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- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion type Assertion NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_head.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion description "[Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion evidence source_evidence_literature NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion SIO_000772 22178368 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion wasDerivedFrom befree-20140225 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.
- NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_assertion wasGeneratedBy ECO_0000203 NP791949.RAyUndkmO9uivcSv4QoLyy6JjWRX8Gd-Tw0VMZp5qvXVA130_provenance.