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- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion type Assertion NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_head.
- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion description "[Mutations in the human alpha-sarcoglycan gene on chromosome 17q21.2 have been shown to cause a severe childhood autosomal recessive muscular dystrophy, a less severe limb girdle muscular dystrophy, exercise intolerance, or asymptomatic hyperCKemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_provenance.
- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion evidence source_evidence_literature NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_provenance.
- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion SIO_000772 14595658 NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_provenance.
- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion wasDerivedFrom befree-20150227 NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_provenance.
- NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_assertion wasGeneratedBy ECO_0000203 NP692016.RALOxNp_wnb4Ya2snzAbud43OM09qCYplPhTiJe1CXE4U130_provenance.