Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion> ?p ?o ?g. }
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- NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion type Assertion NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_head.
- NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion wasGeneratedBy ECO_0000203 NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_provenance.
- NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion wasDerivedFrom befree-2016 NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_provenance.
- NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion SIO_000772 9270600 NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_provenance.
- NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion evidence source_evidence_literature NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_provenance.
- NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_assertion description "[Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1379399.RARRY0EJuvRMDv0QpiHnGwLpozLT5s-Mu_XUoIkST2718130_provenance.