Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion description "[MYH9-related disorders are rare causes of chronic kidney disease (CKD) presenting as chronic glomerulonephritis and derive from mutations of the MYH9 gene, which encodes for the nonmuscle myosin heavy chain IIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion evidence source_evidence_literature NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion SIO_000772 19726116 NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion wasDerivedFrom befree-20140225 NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_assertion wasGeneratedBy ECO_0000203 NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP198352.RAUNyj5PmBwiQxA8_IMa0un_VOFw_gPTu8CVsUEq8wX_E130_provenance.