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- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion type Assertion NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_head.
- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_provenance.
- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion evidence source_evidence_literature NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_provenance.
- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion SIO_000772 21314004 NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_provenance.
- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion wasDerivedFrom befree-20140225 NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_provenance.
- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion wasGeneratedBy ECO_0000203 NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_provenance.