Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_assertion description "[Here we have examined six retinoblastoma patients who are heterozygous for electrophoretic variants of ESD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_assertion evidence source_evidence_literature NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_assertion SIO_000772 6877367 NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_assertion wasDerivedFrom befree-20140225 NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_assertion wasGeneratedBy ECO_0000203 NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP295770.RAkFAupXP8JylQW-FH_yuPIesm4Nab49focAQ67rpoCtg130_provenance.