Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion description "[We hypothesize that most ABCR mutations can be classified in different classes of severity, and that, depending on the remaining total activity of ABCR, the phenotype can range from AMD at the mild end to RP at the severe end of the spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion evidence source_evidence_literature NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion SIO_000772 9810566 NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion wasDerivedFrom befree-20140225 NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_assertion wasGeneratedBy ECO_0000203 NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP177847.RAWPFg2oXH4-jjAjrDaJZ-w-WtEYLI1VA7qw0IeFOdZZM130_provenance.