Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- befree-2016 importedOn "2016-02-19" NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_assertion wasGeneratedBy ECO_0000203 NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_assertion wasDerivedFrom befree-2016 NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_assertion SIO_000772 18294227 NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_assertion evidence source_evidence_literature NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.
- NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_assertion description "[Functional Cathepsin C mutations cause different Papillon-Lefèvre syndrome phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656988.RAlEpKrWsMcFJ4rfE0N7IhS7f-RPV-Gwcw0tmuebY5LT8130_provenance.