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- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion type Assertion NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_head.
- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_provenance.
- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion evidence source_evidence_literature NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_provenance.
- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion SIO_000772 17314340 NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_provenance.
- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion wasDerivedFrom befree-20140225 NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_provenance.
- NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_assertion wasGeneratedBy ECO_0000203 NP808225.RAPv1UpvDEAQh_c2nWaV6n9xVa0nnYrAXL42n5OBRlr8U130_provenance.