Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_assertion description "[Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, phi 2.22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_assertion evidence source_evidence_literature NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_assertion SIO_000772 1975092 NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_assertion wasDerivedFrom befree-20140225 NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_assertion wasGeneratedBy ECO_0000203 NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP672631.RAB733_jSuduU6VWv5ibpwRPekrMnQJ1q34YUQn_kurtA130_provenance.