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- source_evidence_literature type ECO_0000212 NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_assertion wasGeneratedBy ECO_0000203 NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_assertion wasDerivedFrom befree-20150227 NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_assertion SIO_000772 8045710 NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_assertion evidence source_evidence_literature NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.
- NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_assertion description "[Patients from two families, one with a mutation in codon 167 (Gly167Asp) leading to macular degeneration and another with a mutation in codon 210 (Pro210Ser) leading to retinitis pigmentosa, were studied with clinical examinations and measurements of rod and cone sensitivities and dark adaptation, electroretinography, and rhodopsin levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671983.RAXxZrAQUHqSTv2jHrK1s4f_2_aRLBXqjIkdU7tTxsNqA130_provenance.