Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- befree-2016 importedOn "2016-02-19" NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_assertion wasGeneratedBy ECO_0000203 NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_assertion wasDerivedFrom befree-2016 NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_assertion SIO_000772 10817652 NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_assertion evidence source_evidence_literature NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.
- NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_assertion description "[In order to establish a genotype-phenotype correlation, we performed haplotype analysis using microsatellite markers closest to the FCMD gene (FCMD) in 56 Japanese FCMD families, including 35 families whose children were diagnosed as FCMD with the typical phenotype, 12 families with a mild phenotype, and 9 families with a severe phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284396.RA7LGBM8AJFZbp-TeczPAZU8_1kNODP01Mq67BuaIi3gs130_provenance.