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- NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion type Assertion NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_head.
- NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_provenance.
- NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion evidence source_evidence_literature NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_provenance.
- NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion SIO_000772 21829228 NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_provenance.
- NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion wasDerivedFrom befree-20150227 NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_provenance.
- NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_assertion wasGeneratedBy ECO_0000203 NP844806.RAnAvnwJLEzNXlW-u0PCOc3zmtZvXYLCSljnZr8rJll5c130_provenance.