Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_assertion description "[Molecular analysis of the 5 alpha-reductase type 2 gene in a patient with confirmed biochemical 5 alpha-reductase deficiency has resulted in the identification of a novel mutation, GAA to AAA, at codon 200.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_assertion evidence source_evidence_literature NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_assertion SIO_000772 9208814 NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_assertion wasDerivedFrom befree-2016 NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_assertion wasGeneratedBy ECO_0000203 NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1376031.RAiGcKGLxEbc1znaU1AW74ZAdUFxkNUPFtqPrtqQSHmWg130_provenance.