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- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion type Assertion NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_head.
- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_provenance.
- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion evidence source_evidence_literature NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_provenance.
- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion SIO_000772 25848753 NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_provenance.
- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion wasDerivedFrom befree-2016 NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_provenance.
- NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_assertion wasGeneratedBy ECO_0000203 NP1276307.RA3OKL4_99LJ7qdTsYbA_YrjnEo2KT1BfLeoBkAqzWn2w130_provenance.