Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- befree-2016 importedOn "2016-02-19" NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_assertion wasGeneratedBy ECO_0000203 NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_assertion wasDerivedFrom befree-2016 NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_assertion SIO_000772 21929367 NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_assertion evidence source_evidence_literature NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.
- NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_assertion description "[Of the 187 subjects screened, 36 were heterozygous for Hb S [β6(A3)Glu→Val, GAG>GTG] (allele frequency 9.62%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924674.RAFnLF7c_deU_G-J3lTS4SdmzTNYfMV5VbIyusZm3kCn0130_provenance.