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- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion type Assertion NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_head.
- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_provenance.
- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion evidence source_evidence_literature NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_provenance.
- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion SIO_000772 22184204 NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_provenance.
- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion wasDerivedFrom befree-20140225 NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_provenance.
- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion wasGeneratedBy ECO_0000203 NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_provenance.