Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion> ?p ?o ?g. }
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- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion type Assertion NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_head.
- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion description "[Remarkably, two clinically distinct forms of autosomal recessive muscular dystrophy, LGMD type 2B (LGMD2B) and Miyoshi myopathy, were recently mapped to the same locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion evidence source_evidence_literature NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion SIO_000772 9009996 NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion wasDerivedFrom befree-20140225 NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_assertion wasGeneratedBy ECO_0000203 NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.