Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP184552.RAViKEHKZblXxruvB0jwKAY1RrpJP2ITJmKtHc0wbZt00130_provenance.