Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion> ?p ?o ?g. }
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- NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion type Assertion NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_head.
- NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion wasGeneratedBy ECO_0000203 NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion wasDerivedFrom befree-20150227 NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion SIO_000772 7581449 NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion evidence source_evidence_literature NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_assertion description "[Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.