Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP692061.RAfJhbphcxlHAfC7T9rDIdMG44Z9jBzpC1kcr0_HiG6TA130_provenance.
- 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.