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- NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_assertion type Assertion NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_head.
- NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_assertion description "[These data indicate that mutations in SCO2 cause a fatal infantile mitochondrial disorder characterized by hypertrophic cardiomyopathy and encephalopathy, and point to the presence of one or more other genes, perhaps in the copper delivery pathway, in this clinical phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_provenance.
- NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_assertion evidence source_evidence_literature NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_provenance.
- NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_assertion SIO_000772 10749987 NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_provenance.
- NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_assertion wasDerivedFrom befree-20150227 NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_provenance.
- NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_assertion wasGeneratedBy ECO_0000203 NP834251.RA1uCJOQKWSPWUcFSSS_v9D5rA9G9sFXf_wb2J3W0Jii4130_provenance.