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- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion type Assertion NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_head.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion description "[A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion evidence source_evidence_literature NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion SIO_000772 20949531 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion wasDerivedFrom befree-2016 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.
- NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_assertion wasGeneratedBy ECO_0000203 NP845862.RAQbhBxGmIbu-T7dbyfDpjuIr1jMcmDZfTj-CfVLg-AMs130_provenance.