Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_assertion description "[At least 26% and up to 57% of patients with idiopathic perofoveal telangiectasia carry disease-associated variations in the ATM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_assertion evidence source_evidence_literature NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_assertion SIO_000772 18502988 NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_assertion wasDerivedFrom lhgdn-20090331 NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_assertion wasGeneratedBy ECO_0000203 NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211253.RAAUEFWkn-IlJNl-bp5thdU8NBHE3SnYvxd_uPw_Fqulg130_provenance.