Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_assertion description "[We report on the allele distributions in a normal black African population at two microsatellite loci neighbouring the FRAXA locus and at the CGG repeat in the 5' end of the FMR-1 gene, which causes the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_assertion evidence source_evidence_literature NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_assertion SIO_000772 8826479 NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_assertion wasDerivedFrom befree-20140225 NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_assertion wasGeneratedBy ECO_0000203 NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP159946.RABZsACvZ7QvvvgA7w-vwxdJCbE5mAITp1qpfCRchK6C0130_provenance.