Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_assertion description "[Among the cell strains that did not show RDS were two from AT obligate heterozygotes (i.e., the parents of AT patients), two from patients with Alzheimer disease, two from patients with Friedreich ataxia, one from a patient with Bloom syndrome, one from a patient with Down syndrome, and six from patients with various immunodeficiencies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_assertion evidence source_evidence_literature NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_assertion SIO_000772 2722185 NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_assertion wasDerivedFrom befree-20150227 NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_assertion wasGeneratedBy ECO_0000203 NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411369.RAfR7qlVs86w8foY86OiHfhvFc8_GlPL_HaOJBAsjX9IA130_provenance.