Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion> ?p ?o ?g. }
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- NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion type Assertion NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_head.
- NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion description "[Abnormalities of dystrophin are a common cause of muscular dystrophy and testing for dystrophin gene or protein has become a part of routine diagnostic evaluation of patients who present with progressive proximal muscle weakness, high serum creatine kinase concentrations, and histopathological evidence of a dystrophic process.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_provenance.
- NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion evidence source_evidence_literature NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_provenance.
- NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion SIO_000772 11303236 NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_provenance.
- NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion wasDerivedFrom befree-20140225 NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_provenance.
- NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_assertion wasGeneratedBy ECO_0000203 NP271842.RA_gyWUHZoE0Ct-biibBE3hJrMSNidA3SCDAeIAlgOvRQ130_provenance.